Late-onset hereditary spastic paraplegia associated with a genetic variant in interferon induced with helicase c domain 1 (IFIH1) gene.

Zhang, S-Y; Zhu, L; Fan, L-L; Xiang, R; Zeng, L; Jin, J-Y

Zhang, S-Y; Zhu, L; Fan, L-L; Xiang, R; Zeng, L; Jin, J-Y.

Afiliação

Zhang SY; Department of Nephrology, Xiangya Hospital of Central South University, Changsha, 410000, China.
Zhu L; Department of Obstetrics and Gynecology, Ordos Central Hospital, Ordos, 017000, China.
Fan LL; School of Life Sciences, Central South University, Changsha, 410000, China.
Xiang R; School of Life Sciences, Central South University, Changsha, 410000, China.
Zeng L; Department of Orthopaedics, Xiangya Hospital of Central South University, Changsha, 410000, China.
Jin JY; Department of Orthopaedics, Xiangya Hospital of Central South University, Changsha, 410000, China.

QJM ; 116(7): 574-576, 2023 07 28.

Article em En | MEDLINE | ID: mdl-37040079

Assuntos

Interferons; Paraplegia Espástica Hereditária; Humanos; Helicase IFIH1 Induzida por Interferon/genética; Interferons/genética; Paraplegia Espástica Hereditária/genética; Mutação; Linhagem

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Interferons Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: QJM Assunto da revista: MEDICINA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

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