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

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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
Description
ISSN:1432-198X
DOI:10.1007/s00467-015-3067-9