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.
Description
ISSN:1364-6753
DOI:10.1007/s10048-017-0528-2