Targeted Exome Sequencing Integrated with Clinicopathological Information Reveals Novel and Rare Mutations in Atypical, Suspected and Unknown Cases of Alport Syndrome or Proteinuria-Reference-Cited by-同舟云学术

Targeted Exome Sequencing Integrated with Clinicopathological Information Reveals Novel and Rare Mutations in Atypical, Suspected and Unknown Cases of Alport Syndrome or Proteinuria

Published:2013-10-10 Issue:10 Volume:8 Page:e76360
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Chatterjee Rajshekhar,Hoffman Mary,Cliften Paul,Seshan Surya,Liapis Helen,Jain Sanjay

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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4. Significance of proteinuria on the outcome of renal function in patients with focal segmental glomerulosclerosis;JA Velosa;Mayo Clin Proc,1983

5. Thin basement membrane nephropathy;J Savige;Kidney Int,2003

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