Muscular Dystrophy, Congenital, 1C MeSH Supplementary Concept Data 2023

Details
Concepts

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

Muscular Dystrophy, Congenital, 1C Preferred

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