Slow-Channel Congenital Myasthenic Syndrome due to a Novel Mutation in the Acetylcholine Receptor Alpha Subunit in a South Asian: A Case Report (2021)
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/10.3233/jnd-200566
PubMed Identifier: 33216040
Publication URI: http://europepmc.org/abstract/MED/33216040
Type: Journal Article/Review
Parent Publication: Journal of Neuromuscular Diseases
Issue: 1