Slow-Channel Congenital Myasthenic Syndrome due to a Novel Mutation in the Acetylcholine Receptor Alpha Subunit in a South Asian: A Case Report. (2021)

First Author: Gooneratne IK
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

Volume: 8

Parent Publication: Journal of neuromuscular diseases

Issue: 1