A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. (2018)

First Author: Estephan EP

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-018-8736-8

PubMed Identifier: 29383513

Publication URI: http://europepmc.org/abstract/MED/29383513

Type: Journal Article/Review

Volume: 265

Parent Publication: Journal of neurology

Issue: 3

ISSN: 0340-5354