DMD protein, human

Preferred Label : DMD protein, human;

MeSH 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;

MeSH synonym : dystrophin (muscular dystrophy, Duchenne and Becker types) protein, human; Dp116 protein, human;

Is substance : O;

Détails

Origin ID

C484258;

UMLS CUI

C1437024;

MeSH term(s) associated for indexing
- dystrophin [MeSH Descriptor]
Record concept(s)
- DMD protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Dystrophin [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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