Case report: Hereditary spastic paraplegia with a novel homozygous mutation in <i>ZFYVE26</i>.

Lai, Ze-Hua; Liu, Xiao-Ying; Song, Yuan-Yue; Zhou, Hai-Yan; Zeng, Li-Li

Case report: Hereditary spastic paraplegia with a novel homozygous mutation in ZFYVE26.

Lai, Ze-Hua; Liu, Xiao-Ying; Song, Yuan-Yue; Zhou, Hai-Yan; Zeng, Li-Li.

Afiliação

Lai ZH; Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Liu XY; Department of Neurology, Yangpu Hospital, Tongji University School of Medicine, Shanghai, China.
Song YY; Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zhou HY; Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zeng LL; Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Front Neurol ; 14: 1160110, 2023.

Article em En | MEDLINE | ID: mdl-37681008

Palavras-chave

SPG15; ZFYVE26; case report; hereditary spastic paraplegia; novel homozygous mutation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

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