Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. (2020)
Attributed to:
Developmental Disorders: From Diagnosis to Mechanism via Cis-Regulation
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2020.08.013
PubMed Identifier: 32891193
Publication URI: http://europepmc.org/abstract/MED/32891193
Type: Journal Article/Review
Volume: 107
Parent Publication: American journal of human genetics
Issue: 4
ISSN: 0002-9297