Genetics and Pathogenesis of Autosomal Dominant Polycystic Kidney Disease: 20 Years On-Reference-Cited by-同舟云学术

Genetics and Pathogenesis of Autosomal Dominant Polycystic Kidney Disease: 20 Years On

Published:2014-11-24 Issue:12 Volume:35 Page:1393-1406
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Cornec-Le Gall Emilie¹²³,Audrézet Marie-Pierre¹²⁴,Le Meur Yannick²³,Chen Jian-Min¹²⁵,Férec Claude¹²⁴⁵

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale (INSERM); Brest France

2. Faculté de Médecine et des Sciences de la Santé; Université de Bretagne Occidentale; Brest France

3. Service de Néphrologie; Hémodialyse et Transplantation Rénale; Centre Hospitalier Régional Universitaire; Hôpital de la Cavale Blanche; Brest France

4. Laboratoire de Génétique Moléculaire et d'Histocompatibilité; Centre Hospitalier Régional Universitaire; Hôpital Morvan; Brest France

5. Etablissement Français du Sang (EFS)-Bretagne; Brest France

Funder

National Plan for Clinical Research

Société Française de Néphrologie

Institut National de la Santé et de la Recherche Médicale (INSERM), France

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference113 articles.

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3. A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes;Ariza;J Med Genet,1997

4. Autosomal dominant polycystic kidney disease: comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients;Audrézet;Hum Mutat,2012

5. Pkd1 haploinsufficiency increases renal damage and induces microcyst formation following ischemia/reperfusion;Bastos;J Am Soc Nephrol,2009

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