A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia. (2020)
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/brain/awaa120
PubMed Identifier: 32428220
Publication URI: http://europepmc.org/abstract/MED/32428220
Type: Journal Article/Review
Volume: 143
Parent Publication: Brain : a journal of neurology
Issue: 6
ISSN: 0006-8950