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International Journal of Audiology Volume 50, 2011 - Issue 12
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Research Article

Mutational analysis for GJB2, GJB6, and GJB3 genes in Campania within a universal neonatal hearing screening programme

Viviana Chinetti *CEINGE-Biotecnologie Avanzate, Naples, Italy;Unità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Sandra Iossa *CEINGE-Biotecnologie Avanzate, Naples, Italy;Unità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Gennaro AulettaUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Virginia CorvinoUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Maria De LucaUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Francesca De FalcoIRCCS-Fondazione SDN, Naples, Italy
,
Pasquale GianniniUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Giorgio LilliUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Rita MalesciUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Pasquale RiccardiUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
,
Elio MarcianoUnità di Audiologia, Dipartimento di Neuroscienze, Università di Napoli “Federico II”, Naples, Italy
&
Annamaria Franzè *CEINGE-Biotecnologie Avanzate, Naples, Italy;Istituto di Genetica e Biofisica “A. Buzzati Traverso”, C.N.R., Naples, ItalyCorrespondence[email protected]
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Pages 866-870 | Received 15 Oct 2010, Accepted 05 Jul 2011, Published online: 15 Sep 2011

Citations (7)

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Pietro Salvago, Enrico Martines, Eleonora La Mattina, Marianna Mucia, Pietro Sammarco, Federico Sireci & Francesco Martines. (2014) Distribution and phenotype of GJB2 mutations in 102 Sicilian patients with congenital non syndromic sensorineural hearing loss. International Journal of Audiology 53:8, pages 558-563.
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Articles from other publishers (6)

Ashley Satterfield‐Nash, Ayesha Umrigar & Tatiana M. Lanzieri. (2020) Etiology of Prelingual Hearing Loss in the Universal Newborn Hearing Screening Era: A Scoping Review. Otolaryngology–Head and Neck Surgery 163:4, pages 662-670.
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Rita Malesci, Roberta Russo, Carmela Monzillo, Carla Laria, Virginia Corvino, Gennaro Auletta, Achille Iolascon & Annamaria Franzè. (2020) Bimodal strategy for excellent audiological rehabilitation in a subject with a novel nonsense mutation of the SLC26A4 gene: A case report. International Journal of Pediatric Otorhinolaryngology 134, pages 110018.
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Kaitian Chen, Xuan Wu, Ling Zong & Hongyan Jiang. (2018) GJB 3 / GJB 6 screening in GJB 2 carriers with idiopathic hearing loss: Is it necessary? . Journal of Clinical Laboratory Analysis 32:9.
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Annamaria Franzè, Gabriella Esposito, Carmela Di Domenico, Sandra Iossa, Giuliana Sauchelli, Tiziana Fioretti, Michele Cavaliere, Gennaro Auletta, Virginia Corvino, Carla Laria, Rita Malesci, Elio Marciano & Francesco Salvatore. (2016) SLC26A4 genotypes associated with enlarged vestibular aqueduct malformation in south Italian children with sensorineural hearing loss. Clinical Chemistry and Laboratory Medicine (CCLM) 0:0.
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Sandra Iossa, Valerio Costa, Virginia Corvino, Gennaro Auletta, Luigi Barruffo, Stefania Cappellani, Carlo Ceglia, Giovanni Cennamo, Adamo Pio D’Adamo, Alessandra D’Amico, Nilde Di Paolo, Raimondo Forte, Paolo Gasparini, Carla Laria, Barbara Lombardo, Rita Malesci, Andrea Vitale, Elio Marciano & Annamaria Franzè. (2015) Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Molecular Cytogenetics 8:1.
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Dylan K. Chan & Kay W. Chang. (2014) GJB2-associated hearing loss: Systematic review of worldwide prevalence, genotype, and auditory phenotype. The Laryngoscope 124:2, pages E34-E53.
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