View in EDS PDF Full Text

Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.

Saved in:
Bibliographic Details
Title: Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
Authors: Lennon R; Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Michael Smith Building, M13 9PT, Manchester, UK, rachel.lennon@manchester.ac.uk., Stuart HM, Bierzynska A, Randles MJ, Kerr B, Hillman KA, Batra G, Campbell J, Storey H, Flinter FA, Koziell A, Welsh GI, Saleem MA, Webb NJ, Woolf AS
Source: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2015 Sep; Vol. 30 (9), pp. 1459-65. Date of Electronic Publication: 2015 Mar 05.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-198X (Electronic) Linking ISSN: 0931041X NLM ISO Abbreviation: Pediatr Nephrol Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Links:
  – Type: pdflink
Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 25739341
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Lennon+R%22">Lennon R</searchLink>; Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Michael Smith Building, M13 9PT, Manchester, UK, rachel.lennon@manchester.ac.uk.<br /><searchLink fieldCode="AU" term="%22Stuart+HM%22">Stuart HM</searchLink><br /><searchLink fieldCode="AU" term="%22Bierzynska+A%22">Bierzynska A</searchLink><br /><searchLink fieldCode="AU" term="%22Randles+MJ%22">Randles MJ</searchLink><br /><searchLink fieldCode="AU" term="%22Kerr+B%22">Kerr B</searchLink><br /><searchLink fieldCode="AU" term="%22Hillman+KA%22">Hillman KA</searchLink><br /><searchLink fieldCode="AU" term="%22Batra+G%22">Batra G</searchLink><br /><searchLink fieldCode="AU" term="%22Campbell+J%22">Campbell J</searchLink><br /><searchLink fieldCode="AU" term="%22Storey+H%22">Storey H</searchLink><br /><searchLink fieldCode="AU" term="%22Flinter+FA%22">Flinter FA</searchLink><br /><searchLink fieldCode="AU" term="%22Koziell+A%22">Koziell A</searchLink><br /><searchLink fieldCode="AU" term="%22Welsh+GI%22">Welsh GI</searchLink><br /><searchLink fieldCode="AU" term="%22Saleem+MA%22">Saleem MA</searchLink><br /><searchLink fieldCode="AU" term="%22Webb+NJ%22">Webb NJ</searchLink><br /><searchLink fieldCode="AU" term="%22Woolf+AS%22">Woolf AS</searchLink>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%228708728%22">Pediatric nephrology (Berlin, Germany)</searchLink> [Pediatr Nephrol] 2015 Sep; Vol. 30 (9), pp. 1459-65. <i>Date of Electronic Publication: </i>2015 Mar 05.
– 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+International%22">Springer International </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>8708728 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-198X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%220931041X%22">0931041X </searchLink><i>NLM ISO Abbreviation: </i>Pediatr Nephrol <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=25739341
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1007/s00467-015-3067-9
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1459
    Titles:
      – TitleFull: Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Lennon R
      – PersonEntity:
          Name:
            NameFull: Stuart HM
      – PersonEntity:
          Name:
            NameFull: Bierzynska A
      – PersonEntity:
          Name:
            NameFull: Randles MJ
      – PersonEntity:
          Name:
            NameFull: Kerr B
      – PersonEntity:
          Name:
            NameFull: Hillman KA
      – PersonEntity:
          Name:
            NameFull: Batra G
      – PersonEntity:
          Name:
            NameFull: Campbell J
      – PersonEntity:
          Name:
            NameFull: Storey H
      – PersonEntity:
          Name:
            NameFull: Flinter FA
      – PersonEntity:
          Name:
            NameFull: Koziell A
      – PersonEntity:
          Name:
            NameFull: Welsh GI
      – PersonEntity:
          Name:
            NameFull: Saleem MA
      – PersonEntity:
          Name:
            NameFull: Webb NJ
      – PersonEntity:
          Name:
            NameFull: Woolf AS
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 09
              Text: 2015 Sep
              Type: published
              Y: 2015
          Identifiers:
            – Type: issn-electronic
              Value: 1432-198X
          Numbering:
            – Type: volume
              Value: 30
            – Type: issue
              Value: 9
          Titles:
            – TitleFull: Pediatric nephrology (Berlin, Germany)
              Type: main
ResultId 1