Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community-Reference-Cited by-同舟云学术

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Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community

Published:2007-03 Issue:3 Volume:9 Page:180-184
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Frishberg Yaacov,Ben-Neriah Ziva,Suvanto Maija,Rinat Choni,Männikkö Minna,Feinstein Sofia,Becker-Cohen Rachel,Jalanko Hannu,Zlotogora Joel,Kestilä Marjo

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference21 articles.

1. Holmberg C, Tryggvason K, Kestilä M, Jalanko H. Congenital nephrotic syndrome. In: Avner EHW, Niaudet P, editors. Pediatric nephrology. Baltimore: Lippincott Williams & Wilkins, 2004; 503–516.

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