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Factor VII Deficiency Due to Compound Heterozygosity for the p.Leu13Pro Mutation and a Novel Mutation in the HNF4 Binding Region (-58G>C) in the F7 Promoter.
Osaki, Koichi; Sogabe, Yoko; Seki, Ritsuko; Nakamura, Takayuki; Morishige, Satoshi; Oku, Eijiro; Takata, Yuka; Mouri, Fumihiko; Yoshimoto, Koji; Nagafuji, Koji; Okamura, Takashi.
Afiliación
  • Osaki K; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Sogabe Y; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Seki R; Graduate School of Engineering, Hokkai-Gakuen University.
  • Nakamura T; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Morishige S; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Oku E; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Takata Y; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Mouri F; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Yoshimoto K; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Nagafuji K; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
  • Okamura T; Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine.
Kurume Med J ; 67(2.3): 83-89, 2022 Nov 16.
Article en En | MEDLINE | ID: mdl-36123027

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Deficiencia del Factor VII Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Kurume Med J Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Deficiencia del Factor VII Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Kurume Med J Año: 2022 Tipo del documento: Article