Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population-Reference-Cited by-同舟云学术

Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population

Published:2020-11 Issue: Volume:138 Page:110247
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Markova T.G.,Alekseeva N.N.,Mironovich O.L.,Galeeva N.M.,Lalayants M.R.,Bliznetz E.A.,Chibisova S.S.,Polyakov A.V.,Tavartkiladze G.A.

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference36 articles.

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3. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans;Zelante;Hum. Mol. Genet.,1997

4. Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions;Bliznetz;J. Hum. Genet.,2017

5. The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances;Lalaiants;Vestn. Otorinolaringol.,2014

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1. Behavioral characterization of the cochlear amplifier lesion due to loss of function of stereocilin (STRC) in human subjects;Hearing Research;2023-11

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4. Vertiges positionnels paroxystiques bénins récidivants chez deux enfants DFNB16 d’une même fratrie : cas clinique CARE;Annales françaises d'Oto-rhino-laryngologie et de Pathologie Cervico-faciale;2023-06

5. The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population;Biomedicines;2023-02-24