[The audiological analysis in the patients homozygous for the c.-23+1G>A mutation in the GJB2 gene presenting with the loss of hearing in Yakutiya].

Teryutin, F M; Barashkov, N A; Kunel'skaya, N L; Pshennikova, V G; Solov'ev, A V

Teryutin, F M; Barashkov, N A; Kunel'skaya, N L; Pshennikova, V G; Solov'ev, A V.

Afiliación

Teryutin FM; Yakutsk Research Centre of Complex Medical Problems, Yakutsk, Russia, 677010; M.K. AmosovInstitute of Natural Sciences, North-Eastern Federal University, Yakutsk, Russia, 677010.
Barashkov NA; Yakutsk Research Centre of Complex Medical Problems, Yakutsk, Russia, 677010; M.K. AmosovInstitute of Natural Sciences, North-Eastern Federal University, Yakutsk, Russia, 677010.
Kunel'skaya NL; L.I. Sverzhevsky Research Institute of Clinical Otorhinolaryngology, Moscow Health Department, Moscow, Russia, 117152.
Pshennikova VG; Yakutsk Research Centre of Complex Medical Problems, Yakutsk, Russia, 677010; M.K. AmosovInstitute of Natural Sciences, North-Eastern Federal University, Yakutsk, Russia, 677010.
Solov'ev AV; M.K. AmosovInstitute of Natural Sciences, North-Eastern Federal University, Yakutsk, Russia, 677010.

Vestn Otorinolaringol ; 81(1): 19-24, 2016.

Article en Ru | MEDLINE | ID: mdl-26977562

Asunto(s)

Conexinas/genética; Sordera; Pruebas Auditivas/métodos; Adolescente; Niño; Conexina 26; Sordera/diagnóstico; Sordera/etnología; Sordera/genética; Femenino; Humanos; Masculino; Siberia/etnología

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Conexinas / Sordera / Pruebas Auditivas Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Asia Idioma: Ru Revista: Vestn Otorinolaringol Año: 2016 Tipo del documento: Article

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