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Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-up.
Zhang, Weihua; Li, Jiuwei; Zhuo, Xiuwei; Zhou, Ji; Feng, Weixing; Gong, Shuai; Ren, Xiaotun; Ding, Changhong; Han, Tongli; Fang, Fang.
Afiliación
  • Zhang W; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Li J; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Zhuo X; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Zhou J; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Feng W; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Gong S; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Ren X; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Ding C; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Han T; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
  • Fang F; Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China.
Pediatr Investig ; 6(1): 5-10, 2022 Mar.
Article en En | MEDLINE | ID: mdl-35382416
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Pediatr Investig Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Pediatr Investig Año: 2022 Tipo del documento: Article