MeSH Browser

MeSH Supplementary: Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
Unique ID: C563529
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563529
Registry Number: 0
Heading Mapped to: *Myopathies, Nemaline
Frequency: 0
Note: PROM mutation in ACTA1
Date of Entry: 2012/11/05

Myopathy, Actin, Congenital, with Excess of Thin Myofilaments MeSH Supplementary Concept Data 2024