Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. (2018)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2018.08.007

PubMed Identifier: 30266223

Publication URI: http://europepmc.org/abstract/MED/30266223

Type: Journal Article/Review

Volume: 28

Parent Publication: Neuromuscular disorders : NMD

Issue: 11

ISSN: 0960-8966