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Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission. (2020)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcaa174

PubMed Identifier: 33215087

Publication URI: http://europepmc.org/abstract/MED/33215087

Type: Journal Article/Review

Volume: 2

Parent Publication: Brain communications

Issue: 2

ISSN: 2632-1297