MeSH Browser

MeSH Supplementary: ESPN protein, human
Unique ID: C493274
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C493274
Entry Term(s): deafness, autosomal recessive 36 protein, human; espin protein, human
Heading Mapped to: *Microfilament Proteins
Frequency: 18
Note: mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction; RefSeq NM_031475
Source: J Med Genet 2004 Aug;41(8):591-5
Date of Entry: 2004/11/24
Revision Date: 2006/05/17

ESPN protein, human MeSH Supplementary Concept Data 2024