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Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency MeSH Supplementary Concept Data 2025


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 Numbers
0
Heading Mapped to
*Muscular Dystrophies
Frequency
0
Note
mutations in ITGA7
Date of Entry
2012/11/05
Revision Date
2012/11/05
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Preferred
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