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Article

Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.

The Annals of otology, rhinology, and laryngology - 1 Dec 2010

Stankovic Konstantina M, Hennessey Ann Marie, Herrmann Barbara, Mankarious Leila A

Abstract excerpt

OBJECTIVES: We report novel mutations in the POU3F4 gene resulting in congenital X-linked deafness DFN3, and describe the results of cochlear implantation in 4 boys (3 siblings) followed for an average of 3.5 years. METHODS: The diagnosis of DFN3 was made in infant boys on the basis of the radiologic criteria of an underdeveloped modiolus, a wide cochlear fossette, and the presence of all cochlear turns. The...

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Source

Identifiers

PMID: 21250553
DOI: 10.1177/000348941011901205

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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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Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene.PMID 21250553Read ↗

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