ESPN protein, human

Preferred Label : ESPN protein, human;

MeSH note : mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction; RefSeq NM_031475;

MeSH synonym : espin protein, human; deafness, autosomal recessive 36 protein, human;

Is substance : O;

Détails

Origin ID

C493274;

UMLS CUI

C1529077;

MeSH term(s) associated for indexing
- microfilament proteins [MeSH Descriptor]
Record concept(s)
- ESPN 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)
- Espin [NCIt concept]

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

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