GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico-Reference-Cited by-同舟云学术

GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico

Published:2014-12 Issue:12 Volume:78 Page:2107-2112
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Hernández-Juárez Aideé Alejandra,Lugo-Trampe José de Jesús,Campos-Acevedo Luis Daniel,Lugo-Trampe Angel,Treviño-González José Luis,de-la-Cruz-Ávila Israel,Martínez-de-Villarreal Laura Elia

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference57 articles.

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3. A novel p.Leu213X mutation in GJB2 gene in a Portuguese family;Gonçalves;Int. J. Pediatr. Otorhinolaryngol.,2013

4. GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent;Shan;Int. J. Pediatr. Otorhinolaryngol.,2010

5. GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype;Chan;Laryngoscope,2014

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1. Congenital hearing loss: a literature review of the genetic etiology in a Mexican population;Boletín Médico del Hospital Infantil de México;2022-09-14

2. Genetic etiology of non-syndromic hearing loss in Latin America;Human Genetics;2021-10-15

3. Expanded carrier screening for preconception reproductive risk assessment: Prevalence of carrier status in a Mexican population;Prenatal Diagnosis;2020-02-27

4. Analyses of del(GJB6‐D13S1830) and del(GJB6‐D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families;Molecular Genetics & Genomic Medicine;2020-02-17

5. Systematic Review of Pathogenic GJB2 Variants in the Latino Population;Otology & Neurotology;2020-02