Homozygous missense WIPI2 variants cause a congenital disorder of autophagy with neurodevelopmental impairments of variable clinical severity and disease course. (2021)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcab183
PubMed Identifier: 34557665
Publication URI: http://europepmc.org/abstract/MED/34557665
Type: Journal Article/Review
Volume: 3
Parent Publication: Brain communications
Issue: 3
ISSN: 2632-1297