Homozygous WASHC4 variant in two sisters causes a syndromic phenotype defined by dysmorphisms, intellectual disability, profound developmental disorder, and skeletal muscle involvement (2021)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/path.5812
PubMed Identifier: 34599609
Publication URI: http://europepmc.org/abstract/MED/34599609
Type: Journal Article/Review
Parent Publication: The Journal of Pathology
Issue: 1
ISSN: 0022-3417