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Article

Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings.

Clinical genetics - 1 May 2005

Arellano B, Pera A, Ramírez-Camacho R, Villamar M, Trinidad A, García J R, Moreno F, Hernández-Chico C

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Identifiers

PMID: 15811013
DOI: 10.1111/j.1399-0004.2005.00432.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings.PMID 15811013Read ↗

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness.Semantic proximity Read ↗

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SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management.Semantic proximity Read ↗

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Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment.Semantic proximity Read ↗

A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.Semantic proximity Read ↗

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.Semantic proximity Read ↗

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.Semantic proximity Read ↗

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