Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. (2020)

First Author: Connaughton DM
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