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Article

Expression of full-length Cochlin p63s is inner ear specific.

Auris, nasus, larynx - 1 Sept 2005

Li Lishu, Ikezono Tetsuo, Watanabe Atsushi, Shindo Susumu, Pawankar Ruby, Yagi Toshiaki

Abstract excerpt

OBJECTIVE: The COCH gene mutated in DFNA9, murine an autosomal dominant hereditary hearing impairment, encodes Cochlin. Cochlin is also suggested to be the self-antigen of autoimmune sensorineural hearing loss. We previously reported that Cochlin constitutes 70% of the inner ear proteins and is classified into three types of isoform, p63s, p44s, and p40s. To study the specificity of expression of Cochlin isoforms...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15885953
DOI: 10.1016/j.anl.2005.03.012

Genes

COCH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Expression of full-length Cochlin p63s is inner ear specific.PMID 15885953Read ↗

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