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Article

Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.

Archives of otolaryngology--head & neck surgery - 1 Jan 2011

Arnett Jameson, Emery Sarah B, Kim Theresa B, Boerst Angelique K, Lee Kwanghyuk, Leal Suzanne M, Lesperance Marci M

Abstract excerpt

OBJECTIVE: To identify the genetic etiology in a family with autosomal dominant progressive sensorineural hearing loss. DESIGN: Prospective molecular genetic research study. SETTING: Academic genetic research laboratory. PARTICIPANTS: Seventeen members of a family with dominant progressive nonsyndromic sensorineural hearing loss: 9 affected, 6 unaffected, and 2 spouses. INTERVENTIONS: Clinical data from...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21242547
DOI: 10.1001/archoto.2010.234
PMCID: PMC3278911

Genes

KCNQ4

Variants

Provenance

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