Syndrome d’Alport : néphropathie héréditaire associée à des mutations dans les gènes codant les chaînes de collagène de type IV-Reference-Cited by-同舟云学术

Syndrome d’Alport : néphropathie héréditaire associée à des mutations dans les gènes codant les chaînes de collagène de type IV

Published:2016-12 Issue:7 Volume:12 Page:544-551
ISSN:1769-7255
Container-title:Néphrologie & Thérapeutique
language:fr
Short-container-title:Néphrologie & Thérapeutique

Author:

Heidet Laurence,Gubler Marie-Claire

Publisher

Elsevier BV

Subject

Nephrology

Reference92 articles.

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5. Identification of a distinct type IV collagen α chain with restricted kidney distribution and assignment of its gene to the locus of X-linked Alport syndrome;Hostikka;Proc Natl Acad Sci U S A,1990

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