Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. (2019)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2019.03.023

PubMed Identifier: 31051115

Publication URI: http://europepmc.org/abstract/MED/31051115

Type: Journal Article/Review

Volume: 104

Parent Publication: American journal of human genetics

Issue: 5

ISSN: 0002-9297