A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease. (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2022.07.013
PubMed Identifier: 36001086
Publication URI: http://europepmc.org/abstract/MED/36001086
Type: Journal Article/Review
Volume: 24
Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics
Issue: 10
ISSN: 1098-3600