Case report: Novel mutations in the SPG11 gene in a case of autosomal recessive hereditary spastic paraplegia with a thin corpus callosum.

Duan, Ji-Qing; Liu, Hui; Wu, Jia-Qiao

Duan, Ji-Qing; Liu, Hui; Wu, Jia-Qiao.

Afiliación

Duan JQ; Department of Intensive Care Unit, The Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu, China.
Liu H; Department of Intensive Care Unit, The Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu, China.
Wu JQ; Department of Anesthesia, The Third People's Hospital of Chengdu, Affiliated Hospital of Southwest Jiaotong University, Chengdu, China.

Front Integr Neurosci ; 17: 1117617, 2023.

Article en En | MEDLINE | ID: mdl-37035454

Palabras clave

SPG11; case report; gene mutation; hereditary spastic paraplegia; thin corpus

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Integr Neurosci Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

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