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)
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/10.1186/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