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Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter. (2021)

First Author: Rodríguez Cruz PM

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.2020.10.006

PubMed Identifier: 33250374

Publication URI: http://europepmc.org/abstract/MED/33250374

Type: Journal Article/Review

Volume: 31

Parent Publication: Neuromuscular disorders : NMD

Issue: 1

ISSN: 0960-8966