A rare mutation in the COLQ gene causing congenital myasthenic syndrome with remarkable improvement to fluoxetine: 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/10.1016/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