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Article

[Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].

Kulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat - 1 Sept 2003

Düzcan Füsun, Wollnik Bernd, Tepeli Emre, Ardiç F Necdet, Uyguner Oya, Bağci Hüseyin

Abstract excerpt

Autosomal recessive non-syndromic hearing loss is the most common form of inherited childhood deafness. Identification of the responsible gene in this type of hearing loss presents difficulties because of marked genetic heterogenicity and limited clinical presentation. A two-year-old girl was ref...

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Identifiers

PMID: 14699249

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14699249-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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