A recurrent homozygous missense DPM3 variant leads to muscle and brain disease. (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/cge.14208
PubMed Identifier: 35932216
Publication URI: http://europepmc.org/abstract/MED/35932216
Type: Journal Article/Review
Volume: 102
Parent Publication: Clinical genetics
Issue: 6
ISSN: 0009-9163