MeSH Browser

MeSH Supplementary: Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency
Unique ID: C567709
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567709
Entry Term(s): Myopathy, Congenital, Due To Integrin Alpha-7 Deficiency
Registry Number: 0
Heading Mapped to: *Muscular Dystrophies
Frequency: 0
Note: mutations in ITGA7
Date of Entry: 2012/11/05

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency MeSH Supplementary Concept Data 2024