MeSH Browser

MeSH Supplementary: Congenital myasthenic syndrome ib
Unique ID: C536089
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536089
Entry Term(s): Congenital Myasthenic Syndrome Type Ib; Myasthenia, Limb-Girdle, Familial; Myasthenia, familial limb-girdle
Registry Number: 0
Heading Mapped to: *Myasthenic Syndromes, Congenital
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2012/12/03

Congenital myasthenic syndrome ib MeSH Supplementary Concept Data 2024