<i>GJB</i>2 and <i>GJB</i>6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort

<i>GJB</i>2 and <i>GJB</i>6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort

Genetic variants in <i>GJB</i>2 and <i>GJB</i>6 genes are the most frequent causes of hereditary hearing loss among several deaf populations worldwide. Molecular diagnosis enables proper genetic counseling and medical prognosis to patients. In this study, we present an update...

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Bibliographic Details
Main Authors: Paula Buonfiglio, Carlos D. Bruque, Leonela Luce, Florencia Giliberto, Vanesa Lotersztein, Sebastián Menazzi, Bibiana Paoli, Ana Belén Elgoyhen, Viviana Dalamón
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Genes
Subjects:
<i>GJB</i>2
<i>GJB</i>6
genetic variants
curation
hearing loss
argentina
Online Access:https://www.mdpi.com/2073-4425/11/10/1233

Internet

https://www.mdpi.com/2073-4425/11/10/1233

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