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Article

WFS1 mutations in hearing-impaired children.

International journal of audiology - 1 Jul 2014

Häkli Sanna, Kytövuori Laura, Luotonen Mirja, Sorri Martti, Majamaa Kari

Abstract excerpt

OBJECTIVE: Mutations in the WFS1 gene can cause Wolfram syndrome or nonsyndromic hearing impairment (HI). The objective of this study was to ascertain the presence of mutations in WFS1 among children with HI from unknown causes. DESIGN: We screened 105 Finnish children with HI for mutations in ex...

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Source

Identifiers

PMID: 24909696
DOI: 10.3109/14992027.2014.887230

Genes

WFS1
GJB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24909696-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Research trail→

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WFS1 mutations in hearing-impaired children.PMID 24909696Read ↗

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Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.Semantic proximity Read ↗

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.Semantic proximity Read ↗

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