Identification of c.1495C > T mutation in SPAST gene in a family of Han Chinese with hereditary spastic paraplegia.

Chen, Xiaohong; Li, Xinming; Tan, Yu; Yang, Dejiang; Lu, Lijun; Deng, Youqing; Xu, Renshi

Identification of c.1495C > T mutation in SPAST gene in a family of Han Chinese with hereditary spastic paraplegia.

Chen, Xiaohong; Li, Xinming; Tan, Yu; Yang, Dejiang; Lu, Lijun; Deng, Youqing; Xu, Renshi.

Afiliación

Chen X; Department of Neurology, The First Hospital of Nanchang, Nanchang 330006, Jiangxi, China.
Li X; Department of Neurology, The First Hospital of Nanchang, Nanchang 330006, Jiangxi, China.
Tan Y; Department of Neurology, The First Hospital of Nanchang, Nanchang 330006, Jiangxi, China.
Yang D; Department of Neurology, The First Hospital of Nanchang, Nanchang 330006, Jiangxi, China.
Lu L; Department of Neurology, The First Hospital of Nanchang, Nanchang 330006, Jiangxi, China.
Deng Y; Department of Neurology, The First Hospital of Nanchang, Nanchang 330006, Jiangxi, China. Electronic address: youqing1969@126.com.
Xu R; Department of Neurology, Jiangxi Provincial People's Hospital, The Clinical College of Nanchang College, The First Affiliated Hospital of Nanchang College, Nanchang 330006, Jiangxi, China. Electronic address: xurenshi@ncu.edu.cn.

Neurosci Lett ; 812: 137399, 2023 08 24.

Article en En | MEDLINE | ID: mdl-37473796

Asunto(s)

Paraplejía Espástica Hereditaria; Humanos; Masculino; Femenino; Paraplejía Espástica Hereditaria/diagnóstico; Espastina/genética; Pueblos del Este de Asia; Mutación

Palabras clave

Chinese Han nationality; Gene mutation; Genetics; Hereditary spastic paraplegia; SPAST gene

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Neurosci Lett Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Irlanda

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google