Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice

A cohort of 128 patients from 118 families diagnosed with non-syndromic or syndromic hearing loss (HL) underwent an exhaustive clinical evaluation. Molecular analysis was performed using targeted next-generation sequencing (NGS) with a custom panel that included 59 genes associated with non-syndromi...

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Detalles Bibliográficos
Autores principales: García-García, Gema, Berzal-Serrano, Alba, García-Díaz, Piedad, Villanova-Aparisi, Rebeca, Juárez-Rodríguez, Sara, de Paula-Vernetta, Carlos, Cavallé-Garrido, Laura, Jaijo, Teresa, Armengot-Carceller, Miguel, Millán, José M, Aller, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762334/
https://www.ncbi.nlm.nih.gov/pubmed/33297549
http://dx.doi.org/10.3390/genes11121467

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7762334/
https://www.ncbi.nlm.nih.gov/pubmed/33297549
http://dx.doi.org/10.3390/genes11121467

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