MeSH Browser

MeSH Supplementary: WHRN protein, human
Unique ID: C477219
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C477219
Entry Term(s): Autosomal recessive deafness type 31 protein, human; DFNB31 protein, human; deafness, autosomal recessive 31 protein, human; whirlin protein, human
Registry Numbers: 0
Heading Mapped to: *Membrane Proteins
Frequency: 30
Note: RefSeq NM_015404
Source: Nat Genet 2003 Aug;34(4):421-8
Date of Entry: 2003/09/15
Revision Date: 2019/08/27

WHRN protein, human MeSH Supplementary Concept Data 2025