Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features. (2018)

First Author: Turnpenny PD
Attributed to:  Computational Genomics Analysis and Training programme (CGAT) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2018.09.012

PubMed Identifier: 30343942

Publication URI: http://europepmc.org/abstract/MED/30343942

Type: Journal Article/Review

Volume: 103

Parent Publication: American journal of human genetics

Issue: 5

ISSN: 0002-9297