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Article

[Genetic study of hearing loss in families from Argentina].

Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina) - 1 Jan 2004

Reynoso Raúl A, Hendl Silvia, Barteik Marìa E, Curet Carlos A, Nicemboin Luis, Moreno Barral José, Rodríguez Ballesteros Montserrat, Del Castillo Ignacio, Moreno Felipe

Abstract excerpt

Recent advances in molecular genetics as well as improved strategies for the prevention and control of non-syndromic hearing loss (NSHL) have contributed to the rising importance of their inherited causes. In this study we report 32 families from Argentine with one (sporadic) or more (familial) individuals affected. All the families were initially screened for mutations in three autosomal nuclear genes and one...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15366230

Genes

GJB2
GJB6
OTOF

Variants

Provenance

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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