A rare mutation in the COLQ gene causing congenital myasthenic syndrome with remarkable improvement to fluoxetine: A case report. (2021)

First Author: Vidanagamage A
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.2020.12.002

PubMed Identifier: 33487521

Publication URI: http://europepmc.org/abstract/MED/33487521

Type: Journal Article/Review

Volume: 31

Parent Publication: Neuromuscular disorders : NMD

Issue: 3

ISSN: 0960-8966