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Article

MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.

Archives of otolaryngology--head & neck surgery - 1 Aug 2001

Chen A H, Stephan D A, Hasson T, Fukushima K, Nelissen C M, Chen A F, Jun A I, Ramesh A, Van Camp G, Smith R J

Abstract excerpt

BACKGROUND: Earlier studies have mapped the autosomal recessive nonsyndromic deafness locus, DFNB15, to chromosomes 3q21.3-q25.2 and 19p13.3-13.1, identifying one of these chromosomal regions (or possibly both) as the site of a deafness-causing gene. Mutations in unconventional myosins cause deafness in mice and humans. One unconventional myosin, myosin 1F (MYO1F), is expressed in the cochlea and maps to...

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PMID: 11493199
DOI: 10.1001/archotol.127.8.921

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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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