Congenital myasthenic syndrome due to choline acetyltransferase mutations in infants: clinical suspicion and comprehensive electrophysiological assessment are important for early diagnosis. (2014)

First Author: Dilena R
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 23292760

Publication URI:

Type: Journal Article/Review

Volume: 29

Parent Publication: Journal of child neurology

Issue: 3

ISSN: 0883-0738