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Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
Hao, Lili; Li, Shanshan; Ma, Duan; Chen, Shiyu; Zhang, Bowen; Xiao, Deyong; Zhang, Jin; Jiang, Nan; Jiang, Shayi; Ma, Jing.
Afiliação
  • Hao L; Department of Biochemistry and Molecular Biology, Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University, Shanghai, China.
  • Li S; Shanghai Children's Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Ma D; Department of Biochemistry and Molecular Biology, Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University, Shanghai, China.
  • Chen S; Pediatrics Research Institute, Children's Hospital of Fudan University, Shanghai, China.
  • Zhang B; Research Center for Birth Defects, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Xiao D; Shanghai Key Lab of Birth Defect, Children's Hospital of Fudan University, Shanghai, China.
  • Zhang J; Research Center for Birth Defects, Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Jiang N; Department of Biochemistry and Molecular Biology, Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University, Shanghai, China.
  • Jiang S; Department of Biochemistry and Molecular Biology, Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University, Shanghai, China.
  • Ma J; Department of Biochemistry and Molecular Biology, Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University, Shanghai, China.
J Cell Mol Med ; 23(6): 4454-4463, 2019 06.
Article em En | MEDLINE | ID: mdl-31016877
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esferocitose Hereditária / Anquirinas / Povo Asiático / Mutação com Perda de Função Limite: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esferocitose Hereditária / Anquirinas / Povo Asiático / Mutação com Perda de Função Limite: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2019 Tipo de documento: Article