Homozygous mutations in VAMP1 cause a presynaptic congenital myasthenic syndrome. (2017)

First Author: Salpietro V

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/ana.24905

PubMed Identifier: 28253535

Publication URI: http://europepmc.org/abstract/MED/28253535

Type: Journal Article/Review

Volume: 81

Parent Publication: Annals of neurology

Issue: 4

ISSN: 0364-5134