A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report. (2016)

Abstract

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s12883-016-0716-y

PubMed Identifier: 27717316

Publication URI: http://europepmc.org/abstract/MED/27717316

Type: Journal Article/Review

Volume: 16

Parent Publication: BMC neurology

Issue: 1

ISSN: 1471-2377