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Two Novel Heterozygous Mutations (p.γPhe230Val and p.AαAsn839Thr) Cause Hereditary Hypodysfibrinogenemia in Two Chinese Independent Families.
Ge, Shengchen; Luo, Yuqing; Dong, Rujiao; Guo, Xiaoli; Wang, Mingshan; Chen, Yi.
Afiliação
  • Ge S; Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Luo Y; Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Dong R; Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Guo X; Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Wang M; Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Chen Y; Department of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Acta Haematol ; 146(3): 252-258, 2023.
Article em En | MEDLINE | ID: mdl-36599322
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Coagulação Sanguínea / Afibrinogenemia Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos da Coagulação Sanguínea / Afibrinogenemia Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article