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Identification of a VHL gene mutation in a Chinese family with Von Hippel­Lindau syndrome.
He, Zhengwen; Xia, Lu; Deng, Zhiyong; Lian, Aojie; Hu, Zhengmao; Li, Bin.
Afiliación
  • He Z; Department of Neurosurgery, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya, School of Medicine, Central South University, Changsha, Hunan 410008, P.R. China.
  • Xia L; Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, P.R. China.
  • Deng Z; Department of Neurosurgery, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya, School of Medicine, Central South University, Changsha, Hunan 410008, P.R. China.
  • Lian A; Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, P.R. China.
  • Hu Z; Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410008, P.R. China.
  • Li B; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.
Mol Med Rep ; 18(1): 435-440, 2018 Jul.
Article en En | MEDLINE | ID: mdl-29749453
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Mutación Missense / Proteína Supresora de Tumores del Síndrome de Von Hippel-Lindau / Enfermedad de von Hippel-Lindau Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Mol Med Rep Año: 2018 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Mutación Missense / Proteína Supresora de Tumores del Síndrome de Von Hippel-Lindau / Enfermedad de von Hippel-Lindau Tipo de estudio: Diagnostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Mol Med Rep Año: 2018 Tipo del documento: Article