A novel SPAST frameshift mutation in a Chinese family with hereditary spastic paraplegia.

Yuliang, Wang; Yuan, Wang; Xuezhen, Wang; He, Ma; Qi, Zheng; Jinbo, Chen

Yuliang, Wang; Yuan, Wang; Xuezhen, Wang; He, Ma; Qi, Zheng; Jinbo, Chen.

Afiliação

Yuliang W; Department of Neurology, Binzhou Medical University Hospital, No. 661 Huanghe 2nd Road of Binzhou, Shandong, China.
Yuan W; Department of Neurology, Binzhou Medical University Hospital, No. 661 Huanghe 2nd Road of Binzhou, Shandong, China.
Xuezhen W; Department of Neurology, Binzhou Medical University Hospital, No. 661 Huanghe 2nd Road of Binzhou, Shandong, China.
He M; Department of Neurology, Binzhou Medical University Hospital, No. 661 Huanghe 2nd Road of Binzhou, Shandong, China.
Qi Z; Department of Neurology, Binzhou Medical University Hospital, No. 661 Huanghe 2nd Road of Binzhou, Shandong, China.
Jinbo C; Department of Neurology, Binzhou Medical University Hospital, No. 661 Huanghe 2nd Road of Binzhou, Shandong, China. chenjinbo6720@126.com.

Neurol Sci ; 38(2): 365-367, 2017 Feb.

Article em En | MEDLINE | ID: mdl-27629539

Assuntos

Adenosina Trifosfatases/genética; Paraplegia Espástica Hereditária/genética; Idoso; China; Mutação da Fase de Leitura; Humanos; Masculino; Linhagem; Espastina

Palavras-chave

Frameshift mutation; Hereditary spastic paraplegia; Ischemic stroke; SPAST

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Adenosina Trifosfatases Limite: Aged / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Neurol Sci Assunto da revista: NEUROLOGIA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China

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