Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies. (2021)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41436-021-01260-4

PubMed Identifier: 34244665

Publication URI: http://europepmc.org/abstract/MED/34244665

Type: Journal Article/Review

Volume: 23

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 11

ISSN: 1098-3600