MeSH Browser

MeSH Supplementary: PDZD7 protein, human
Unique ID: C000611545
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000611545
Entry Term(s): PDZ domain containing 7 protein, human
Registry Numbers: 0
Heading Mapped to: *Carrier Proteins
Frequency: 11
Note: mutations are linked to autosomal recessive non-syndromic hearing loss (ARNSHL); RefSeq NM_001195263
Source: Am J Med Genet A. 2015 Dec;167A(12):2957-65
Date of Entry: 2016/10/14
Revision Date: 2016/10/14

PDZD7 protein, human MeSH Supplementary Concept Data 2025