AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range. (2022)
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/10.1016/j.ejmg.2022.104620
PubMed Identifier: 36122674
Publication URI: http://europepmc.org/abstract/MED/36122674
Type: Journal Article/Review
Volume: 65
Parent Publication: European journal of medical genetics
Issue: 11
ISSN: 1769-7212