Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy. (2014)

First Author: Herrmann DN
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 25192047

Publication URI:

Type: Journal Article/Review

Volume: 95

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297