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[Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene].
Hu, Wenjing; Ling, Xiuxin; Fang, Hongjun; Tang, Jingwen; Kang, Qingyun; Yang, Haiyan; Wu, Liwen.
Afiliación
  • Hu W; Department of Neurology, Hunan Provincial Children's Hospital, Changsha, Hunan 410007, China. 271417152@qq.com.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 40(4): 413-418, 2023 Apr 10.
Article en Zh | MEDLINE | ID: mdl-36972934

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans Idioma: Zh Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Mitocondriales Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans Idioma: Zh Año: 2023 Tipo del documento: Article