LRP5 variants may contribute to ADPKD

Volume: 24, Issue: 2, Pages: 237 - 242
Published: Apr 29, 2015
Abstract
Mutations in Polycystic Kidney Disease proteins (PKD1 or PKD2) are causative for autosomal dominant polycystic kidney disease (ADPKD). However, a small subset of ADPKD probands do not harbor a mutation in any of the known genes. Low density lipoprotein Receptor-related Protein 5 (LRP5) was recently associated with hepatic cystogenesis in isolated polycystic liver disease (PCLD). Here, we demonstrate that this gene may also have a role in...
Paper Details
Title
LRP5 variants may contribute to ADPKD
Published Date
Apr 29, 2015
Volume
24
Issue
2
Pages
237 - 242
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