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Novel pathogenic ALG2 mutation causing congenital myasthenic syndrome: A case report. (2022)

First Author: Ehrstedt C

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