Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2. A model of early-onset and fast cyst progression.

This article is protected by copyright. All rights reserved.
PMID: 32166738 [PubMed - as supplied by publisher]

Source: Clinical Genetics - March 12, 2020 Category: Genetics & Stem Cells Authors: Peces R, Mena R, Peces C, Cuesta E, Selgas R, Barruz P, Lapunzina P, Nevado J Tags: Clin Genet Source Type: research