Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report. (2022)
Attributed to:
Disease mechanisms and therapy for inherited disorders of the neuromuscular synapse.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2021.11.012
PubMed Identifier: 34980536
Publication URI: http://europepmc.org/abstract/MED/34980536
Type: Journal Article/Review
Volume: 32
Parent Publication: Neuromuscular disorders : NMD
Issue: 1
ISSN: 0960-8966