Han Chinese family with early-onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene.

Huang, Ting; Gao, Chen-Yu; Wu, Liang; Gong, Peng-Yu; Wang, Ji-Zheng; Tian, You-Yong; Zhang, Ying-Dong

Huang, Ting; Gao, Chen-Yu; Wu, Liang; Gong, Peng-Yu; Wang, Ji-Zheng; Tian, You-Yong; Zhang, Ying-Dong.

Afiliación

Huang T; Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Gao CY; Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Wu L; Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Gong PY; Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Wang JZ; Department of Endocrine and Metabolic Diseases, The First People's Hospital of Hefei, Anhui Medical University, Hefei, China.
Tian YY; Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Zhang YD; Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.

Brain Behav ; 9(9): e01372, 2019 09.

Article en En | MEDLINE | ID: mdl-31386307

Asunto(s)

Pueblo Asiatico/genética; Mutación/genética; Enfermedad de Parkinson/genética; Ubiquitina-Proteína Ligasas/genética; Adulto; China; Femenino; Humanos; Masculino; Persona de Mediana Edad; Adulto Joven

Palabras clave

Parkin gene (PARK2); deletion mutations; duplication mutations; early-onset Parkinson's disease

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Ubiquitina-Proteína Ligasas / Pueblo Asiatico / Mutación Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Brain Behav Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

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