a-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism. (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/10.1002/mds.28735
PubMed Identifier: 34543462
Publication URI: http://europepmc.org/abstract/MED/34543462
Type: Journal Article/Review
Volume: 36
Parent Publication: Movement disorders : official journal of the Movement Disorder Society
Issue: 9
ISSN: 0885-3185