Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project. (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/10.1038/s41431-020-00720-w
PubMed Identifier: 32934340
Publication URI: http://europepmc.org/abstract/MED/32934340
Type: Journal Article/Review
Volume: 28
Parent Publication: European journal of human genetics : EJHG
Issue: 12
ISSN: 1018-4813