Your browser doesn't support javascript.
loading
Early Onset of Combined Oxidative Phosphorylation Deficiency in Two Chinese Brothers Caused by a Homozygous (Leu275Phe) Mutation in the C1QBP Gene.
Wang, Jie; Li, Huan; Sun, Min; Yang, Ying; Yang, Qianli; Liu, Bailing; Liu, Fang; Hu, Wen; Zhang, Yanmin.
Afiliação
  • Wang J; Shaanxi Institute for Pediatric Diseases, Xi'an Children's Hospital, Xi'an, China.
  • Li H; Xi'an Key Laboratory of Children's Health and Diseases, Xi'an, China.
  • Sun M; Xi'an Key Laboratory of Children's Health and Diseases, Xi'an, China.
  • Yang Y; Department of Cardiology of Xi'an Children's Hospital, Affiliated Children's Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Yang Q; Department of Cardiology of Xi'an Children's Hospital, Affiliated Children's Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Liu B; Shaanxi Institute for Pediatric Diseases, Xi'an Children's Hospital, Xi'an, China.
  • Liu F; Xi'an Key Laboratory of Children's Health and Diseases, Xi'an, China.
  • Hu W; Department of Ultrasound, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
  • Zhang Y; Department of Ultrasound of Xi'an Children's Hospital, Affiliated Children's Hospital of Xi'an Jiaotong University, Xi'an, China.
Front Pediatr ; 8: 583047, 2020.
Article em En | MEDLINE | ID: mdl-33344382

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pediatr Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China