The polyG diseases: a new disease entity.

Liufu, Tongling; Zheng, Yilei; Yu, Jiaxi; Yuan, Yun; Wang, Zhaoxia; Deng, Jianwen; Hong, Daojun

Liufu, Tongling; Zheng, Yilei; Yu, Jiaxi; Yuan, Yun; Wang, Zhaoxia; Deng, Jianwen; Hong, Daojun.

Afiliación

Liufu T; Department of Neurology, Peking University First Hospital, Beijing, China.
Zheng Y; Department of Neurology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yu J; Department of Neurology, Peking University First Hospital, Beijing, China.
Yuan Y; Department of Neurology, Peking University First Hospital, Beijing, China.
Wang Z; Department of Neurology, Peking University First Hospital, Beijing, China.
Deng J; Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.
Hong D; Department of Neurology, Peking University First Hospital, Beijing, China. jianwendeng@pkufh.com.

Acta Neuropathol Commun ; 10(1): 79, 2022 05 31.

Article en En | MEDLINE | ID: mdl-35642014

Asunto(s)

Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil; Síndrome del Cromosoma X Frágil; Ataxia/complicaciones; Síndrome del Cromosoma X Frágil/patología; Humanos; Cuerpos de Inclusión Intranucleares; Distrofias Musculares; Enfermedades Neurodegenerativas; Péptidos; Temblor

Palabras clave

Fragile X-associated tremor/ataxia syndrome; Neuronal intranuclear inclusion disease; Oculopharyngeal myopathy with leukoencephalopathy; Oculopharyngodistal myopathy; PolyG diseases

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil Límite: Humans Idioma: En Revista: Acta Neuropathol Commun Año: 2022 Tipo del documento: Article País de afiliación: China

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