Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy

被引：0
|
作者：
Stefanie Weber
Katja Strasser
Sabine Rath
Achim Kittke
Sonja Beicht
Martin Alberer
Bärbel Lange-Sperandio
Peter F. Hoyer
Marcus R. Benz
Sabine Ponsel
Lutz T. Weber
Hanns-Georg Klein
Julia Hoefele
机构：
[1] University of Duisburg-Essen,Pediatric Nephrology, Pediatrics II
[2] Center for Human Genetics and Laboratory Diagnostics Dr. Klein,Department of Infectious Diseases and Tropical Medicine
[3] Dr. Rost and Colleagues,Pediatric Nephrology, University Children’s Hospital
[4] Ludwig-Maximilians University,Pediatric Nephrology
[5] Ludwig-Maximilians University,Institute of Human Genetics
[6] University Children’s Hospital,undefined
[7] Technische Universität München,undefined
来源：
Pediatric Nephrology | 2016年 / 31卷
关键词：
Alport syndrome; Thin basement membrane nephropathy; Mutational analysis;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：941 / 955
页数：14
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