Myotilinopathy MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Myotilinopathy
Unique ID: C563775
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563775
Entry Term(s): Myopathy, Myofibrillar, Myotilin-Related
Registry Number: 0
Heading Mapped to: *Myopathies, Structural, Congenital
Frequency: 4
Note: mutation in myotilin
Date of Entry: 2012/11/05

Myotilinopathy Preferred

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