[Hearing loss due to mutations in the genes responsible for Usher syndrome].

Markova, T G; Alekseeva, N N; Belov, O A; Chugunova, T I; Tsygankova, E R

[Hearing loss due to mutations in the genes responsible for Usher syndrome]. / Narushenie slukha pri mutatsiyakh v genakh, otvetstvennykh za sindrom Ashera.

Markova, T G; Alekseeva, N N; Belov, O A; Chugunova, T I; Tsygankova, E R.

Afiliación

Markova TG; National Research Centre for Audiology and Hearing Rehabilitation, Moscow, Russia.
Alekseeva NN; Russian Medical Academy for Continuous Professional Education Audiology Department, Moscow, Russia.
Belov OA; National Research Centre for Audiology and Hearing Rehabilitation, Moscow, Russia.
Chugunova TI; Russian Medical Academy for Continuous Professional Education Audiology Department, Moscow, Russia.
Tsygankova ER; National Research Centre for Audiology and Hearing Rehabilitation, Moscow, Russia.

Vestn Otorinolaringol ; 87(1): 52-59, 2022.

Article en Ru | MEDLINE | ID: mdl-35274893

Asunto(s)

Retinitis Pigmentosa; Síndromes de Usher; Niño; Pruebas Auditivas; Humanos; Mutación; Retinitis Pigmentosa/genética; Síndromes de Usher/diagnóstico; Síndromes de Usher/genética

Palabras clave

MYO7A; USH2A genes; Usher syndrome; hereditary hearing loss/deafness; syndromal and nonsyndromal sensorineural hearing loss

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retinitis Pigmentosa / Síndromes de Usher Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: Ru Revista: Vestn Otorinolaringol Año: 2022 Tipo del documento: Article País de afiliación: Rusia Pais de publicación: Rusia

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