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Article

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.

The Laryngoscope - 1 Apr 2009

Shearer A Eliot, Hildebrand Michael S, Webster Jennifer A, Kahrizi Kimia, Meyer Nicole C, Jalalvand Khadijeh, Arzhanginy Sanaz, Kimberling William J, Stephan Dietrich, Bahlo Melanie, Smith Richard J H, Najmabadi Hossein

Abstract excerpt

OBJECTIVES: To use clinical and genetic analyses to determine the mutation causing autosomal recessive nonsyndromic hearing loss (ARNSHL) segregating in two consanguineous Iranian families. STUDY DESIGN: Family study. METHODS: Members of each family received otologic and audiometric examination for the type and extent of hearing loss. Linkage mapping using Affymetrix 50K GeneChips and short tandem repeat (STRP)...

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Share to Chromosomes, Human, Pair 17
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss, Sensorineural

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Share to Mutation, Missense

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Share to Sequence Analysis, Protein

Source

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Identifiers

PMID: 19274735
DOI: 10.1002/lary.20116
PMCID: PMC2885251

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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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Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.PMID 19274735Read ↗

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