Screening forGJB2andGJB6gene mutations in patients from Campania region with sensorineural hearing loss-Reference-Cited by-同舟云学术

Screening forGJB2andGJB6gene mutations in patients from Campania region with sensorineural hearing loss

Published:2010-01 Issue:4 Volume:49 Page:326-331
ISSN:1499-2027
Container-title:International Journal of Audiology
language:en
Short-container-title:International Journal of Audiology

Author:

Chinetti Viviana,Iossa Sandra,Auletta Gennaro,Laria Carla,de Luca Maria,Di Leva Francesca,Riccardi Pasquale,Giannini Pasquale,Gasparini Paolo,Ciccodicola Alfredo,Marciano Elio,Franzè Annamaria

Publisher

Informa UK Limited

Subject

Speech and Hearing,Linguistics and Language,Language and Linguistics

Link

http://www.tandfonline.com/doi/pdf/10.3109/14992021003601756

Reference31 articles.

1. Pathogenetic role of the deafness-related M34T mutation of Cx26

2. A genotype-phenotype correlation for GJB2 (connexin 26) deafness

3. Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort

4. A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment

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1. Genetic etiology of non-syndromic hearing loss in Europe;Human Genetics;2022-01-19

2. SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss;Clinical Chemistry and Laboratory Medicine (CCLM);2016-01-19

3. Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss;Molecular Cytogenetics;2015-03-20

4. GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype;The Laryngoscope;2013-10-08

5. Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey;The Journal of Laryngology & Otology;2012-11-22