Long-term follow-up in patients with congenital myasthenic syndrome due to RAPSN mutations. (2016)

First Author: Natera-De Benito D
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2015.10.013

PubMed Identifier: 26782015

Publication URI: http://europepmc.org/abstract/MED/26782015

Type: Journal Article/Review

Volume: 26

Parent Publication: Neuromuscular disorders : NMD

Issue: 2

ISSN: 0960-8966