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

First Author: Herrmann DN

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2014.08.007

PubMed Identifier: 25192047

Publication URI: http://europepmc.org/abstract/MED/25192047

Type: Journal Article/Review

Volume: 95

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297