Mitochondrial mutations in maternally inherited hearing loss.

Mutai, Hideki; Watabe, Takahisa; Kosaki, Kenjiro; Ogawa, Kaoru; Matsunaga, Tatsuo

Mutai, Hideki; Watabe, Takahisa; Kosaki, Kenjiro; Ogawa, Kaoru; Matsunaga, Tatsuo.

Afiliación

Mutai H; Division of Hearing and Balance Research, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, 2-5-1 Higashigaoka, Meguro, Tokyo, 152-8902, Japan.
Watabe T; Department of Otolaryngology, Head and Neck Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, 160-8582, Japan.
Kosaki K; Center for Medical Genetics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, 160-8582, Japan.
Ogawa K; Department of Otolaryngology, Head and Neck Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, 160-8582, Japan.
Matsunaga T; Division of Hearing and Balance Research, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, 2-5-1 Higashigaoka, Meguro, Tokyo, 152-8902, Japan. matsunagatatsuo@kankakuki.go.jp.

BMC Med Genet ; 18(1): 32, 2017 03 20.

Article en En | MEDLINE | ID: mdl-28320335

Asunto(s)

ADN Mitocondrial/genética; Pérdida Auditiva Sensorineural/genética; Mutación; Adulto; Niño; Femenino; Humanos; Masculino; Herencia Materna; Mitocondrias/genética; Análisis de Secuencia de ADN/métodos; Adulto Joven

Palabras clave

MTTS1; Maternal inheritance; Mitochondrial deafness

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ADN Mitocondrial / Pérdida Auditiva Sensorineural / Mutación Tipo de estudio: Prognostic_studies Límite: Adult / Child / Female / Humans / Male Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Japón

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