Prevalence of 35delG mutation in GJB2 gene in the Moldovan population

Background: Guanine deletion 35delG in GJB2 exon 2 is the pathogenic mutation responsible for up to 70% of cases of congenital non-syndromic sensorineural hearing loss (NSHL) among Europeans. The early molecular diagnostic of hearing loss nature has become important while considering the cochlear im...

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Bibliographic Details
Main Authors: Anastasia Buza, Sergiu Parii, Cristina Butovscaia, Daniela Galea-Abdusa, Luminita Radulescu, Ghenadie Curocichin
Format: Article
Language:English
Published: Scientific Medical Association of Moldova 2020-10-01
Series:The Moldovan Medical Journal
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Online Access:http://moldmedjournal.md/wp-content/uploads/2020/10/moldovan-med-j-2020-63-6-buza-et-al-full-text.pdf

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