MeSH Browser

MeSH Supplementary: DMD protein, human
Unique ID: C484258
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C484258
Entry Term(s): Dp116 protein, human; dystrophin (muscular dystrophy, Duchenne and Becker types) protein, human
Registry Numbers: 0
Heading Mapped to: *Dystrophin
Frequency: 349
Note: Defects in DMD are the cause of DUCHENNE MUSCULAR DYSTROPHY (DMD); expressed during embryogenesis; may play a role in anchoring the cytoskeleton to the plasma membrane; RefSeq NM_004006
Date of Entry: 2004/08/06
Revision Date: 2005/09/20

DMD protein, human MeSH Supplementary Concept Data 2025