ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.

Saved in:
Bibliographic Details
Title: ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.
Authors: Wang JY; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Zhou P; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Wang J; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Tang B; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Su T; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Liu XR; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Li BM; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Meng H; Department of Neurology, The First Affiliated Hospital of Jinan University, Guangdong, 510630, China.; Clinical Neuroscience Institute of Jinan University, Guangdong, 510630, China., Shi YW; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., Yi YH; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China., He N; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China. hena@gzhmu.edu.cn.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China. hena@gzhmu.edu.cn., Liao WP; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China. wpliao@163.net.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China. wpliao@163.net.
Source: Neurogenetics [Neurogenetics] 2018 Jan; Vol. 19 (1), pp. 9-16. Date of Electronic Publication: 2017 Nov 13.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1364-6753 (Electronic) Linking ISSN: 13646745 NLM ISO Abbreviation: Neurogenetics Subsets: MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 29130122
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Wang+JY%22">Wang JY</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Zhou+P%22">Zhou P</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Wang+J%22">Wang J</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Tang+B%22">Tang B</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Su+T%22">Su T</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Liu+XR%22">Liu XR</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Li+BM%22">Li BM</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Meng+H%22">Meng H</searchLink>; Department of Neurology, The First Affiliated Hospital of Jinan University, Guangdong, 510630, China.; Clinical Neuroscience Institute of Jinan University, Guangdong, 510630, China.<br /><searchLink fieldCode="AU" term="%22Shi+YW%22">Shi YW</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22Yi+YH%22">Yi YH</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China.<br /><searchLink fieldCode="AU" term="%22He+N%22">He N</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China. hena@gzhmu.edu.cn.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China. hena@gzhmu.edu.cn.<br /><searchLink fieldCode="AU" term="%22Liao+WP%22">Liao WP</searchLink>; Institute of Neuroscience and Department of Neurology of the Second Affiliated Hospital of Guangzhou Medical University Please check if the affiliations are presented correctly.The affiliations are presented correctly., Chang-Gang-Dong Road 250, Guangzhou, 510260, China. wpliao@163.net.; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, 510260, China. wpliao@163.net.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229709714%22">Neurogenetics</searchLink> [Neurogenetics] 2018 Jan; Vol. 19 (1), pp. 9-16. <i>Date of Electronic Publication: </i>2017 Nov 13.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Research Support, Non-U.S. Gov't
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer-Verlag%22">Springer-Verlag </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9709714 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1364-6753 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2213646745%22">13646745 </searchLink><i>NLM ISO Abbreviation: </i>Neurogenetics <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=29130122
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1007/s10048-017-0528-2
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 9
    Titles:
      – TitleFull: ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Wang JY
      – PersonEntity:
          Name:
            NameFull: Zhou P
      – PersonEntity:
          Name:
            NameFull: Wang J
      – PersonEntity:
          Name:
            NameFull: Tang B
      – PersonEntity:
          Name:
            NameFull: Su T
      – PersonEntity:
          Name:
            NameFull: Liu XR
      – PersonEntity:
          Name:
            NameFull: Li BM
      – PersonEntity:
          Name:
            NameFull: Meng H
      – PersonEntity:
          Name:
            NameFull: Shi YW
      – PersonEntity:
          Name:
            NameFull: Yi YH
      – PersonEntity:
          Name:
            NameFull: He N
      – PersonEntity:
          Name:
            NameFull: Liao WP
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 01
              Text: 2018 Jan
              Type: published
              Y: 2018
          Identifiers:
            – Type: issn-electronic
              Value: 1364-6753
          Numbering:
            – Type: volume
              Value: 19
            – Type: issue
              Value: 1
          Titles:
            – TitleFull: Neurogenetics
              Type: main
ResultId 1