Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2021.11.016
PubMed Identifier: 34890546
Publication URI: http://europepmc.org/abstract/MED/34890546
Type: Journal Article/Review
Parent Publication: The American Journal of Human Genetics
Issue: 1
ISSN: 0002-9297