MeSH Browser

MeSH Supplementary: Endplate Acetylcholinesterase Deficiency
Unique ID: C566415
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566415
Entry Term(s): Congenital Myasthenic Syndrome Type Ic; Engel Congenital Myasthenic Syndrome; Myasthenic Syndrome, Congenital, Engel Type
Registry Numbers: 0
Heading Mapped to: *Myasthenic Syndromes, Congenital
Frequency: 8
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Endplate Acetylcholinesterase Deficiency MeSH Supplementary Concept Data 2025