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A novel SPTB gene mutation in neonatal hereditary spherocytosis: A case report.
Liu, Yang; Zheng, Jie; Song, Li; Fang, Yulian; Sun, Chao; Li, Na; Liu, Geli; Shu, Jianbo.
Affiliation
  • Liu Y; Department of Neonatalogy, Tianjin Children's Hospital, The Pediatric Clinical College in Tianjin Medical University, Tianjin 300074, P.R. China.
  • Zheng J; Graduate College of Tianjin Medical University, Tianjin 300070, P.R. China.
  • Song L; Department of Neonatalogy, Tianjin Children's Hospital, The Pediatric Clinical College in Tianjin Medical University, Tianjin 300074, P.R. China.
  • Fang Y; Tianjin Key Laboratory of Prevention and Treatment of Birth Defects, Tianjin 300134, P.R. China.
  • Sun C; Tianjin Pediatric Research Institute, Tianjin Children's Hospital, Tianjin 300134, P.R. China.
  • Li N; Department of Neonatalogy, Tianjin Children's Hospital, The Pediatric Clinical College in Tianjin Medical University, Tianjin 300074, P.R. China.
  • Liu G; Department of Neonatalogy, Tianjin Children's Hospital, The Pediatric Clinical College in Tianjin Medical University, Tianjin 300074, P.R. China.
  • Shu J; Department of Pediatrics, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.
Exp Ther Med ; 20(4): 3253-3259, 2020 Oct.
Article in En | MEDLINE | ID: mdl-32855695
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Exp Ther Med Year: 2020 Document type: Article Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Exp Ther Med Year: 2020 Document type: Article Country of publication: