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Article

Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).

Archives of otolaryngology--head & neck surgery - 1 Apr 2003

Pennings Ronald J E, Bom Steven J H, Cryns Kim, Flothmann Kris, Huygen Patrick L M, Kremer Hannie, Van Camp Guy, Cremers Cor W R J

Abstract excerpt

OBJECTIVE: To assess the audiometric profile and speech recognition characteristics in affected members of 2 families with DFNA6/14 harboring heterozygous mutations in the WFS1 gene that cause an autosomal dominant nonsyndromic sensorineural hearing impairment trait. DESIGN: Family study. SETTING: Tertiary referral center. Patients Thirteen patients from 2 recently identified Dutch families with DFNA6/14 (Dutch...

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Source

Identifiers

PMID: 12707188
DOI: 10.1001/archotol.129.4.421

Genes

WFS1

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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