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Article

Are MYO1C and MYO1F associated with hearing loss?

Biochimica et biophysica acta - 1 Jan 2009

Zadro Cristina, Alemanno Maria Stella, Bellacchio Emanuele, Ficarella Romina, Donaudy Francesca, Melchionda Salvatore, Zelante Leopoldo, Rabionet Raquel, Hilgert Nele, Estivill Xavier, Van Camp Guy, Gasparini Paolo, Carella Massimo

Abstract excerpt

The role of myosins in the pathogenesis of hearing loss is well established: five genes encoding unconventional myosins and two genes encoding nonmuscle conventional myosins have so far been described to be essential for normal auditory function and mutations in these genes associated with hearing impairment. To better understand the role of this gene family we performed a mutational screening on two candidate...

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Share to Heterozygote
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Myosin Type I

Share to DNA Mutational Analysis

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Share to Hearing Loss, Sensorineural

Share to Protein Structure, Tertiary

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Identifiers

PMID: 19027848
DOI: 10.1016/j.bbadis.2008.10.017

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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