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Article

GJB2 (Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort.

Acta oto-laryngologica - 1 Dec 2012

Carlsson Per-Inge, Karltorp Eva, Carlsson-Hansén Eva, Åhlman Henrik, Möller Claes, Vondöbeln Ulrika

Abstract excerpt

CONCLUSION: The most common mutation in the Swedish population was Connexin 26 (C×26) 35delG, which indicates that the percentage of Swedish persons with C×26 mutations and polymorphisms in the GJB2 gene among non-syndromic hearing-impaired (HI) persons is comparable to the rest of Europe. The results strongly support a Swedish policy to offer all children with diagnosed hearing impairment genetic tests for the...

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Identifiers

PMID: 23039283
DOI: 10.3109/00016489.2012.701018

Genes

GJB2

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