Muscular Dystrophy, Congenital, 1C MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Muscular Dystrophy, Congenital, 1C
Unique ID: C564691
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564691
Registry Numbers: 0
Heading Mapped to: *Muscular Dystrophies
Frequency: 5
Note: mutation in FKRP
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Muscular Dystrophy, Congenital, 1C Preferred

page delivered in 0.004s