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A case of thrombomodulin mutation causing defective thrombin binding with absence of protein C and TAFI activation.
Okada, Masahiko; Tominaga, Norio; Honda, Goichi; Nishioka, Junji; Akita, Nobuyuki; Hayashi, Tatsuya; Suzuki, Koji; Moriuchi, Hiroyuki.
Afiliación
  • Okada M; Department of Pediatrics, Nagasaki University Hospital, Nagasaki, Japan.
  • Tominaga N; Department of Pediatrics, Nagasaki University Hospital, Nagasaki, Japan.
  • Honda G; Department of Medical Affairs, Asahi Kasei Pharma Corporation, Tokyo, Japan.
  • Nishioka J; Department of Clinical Nutrition, Faculty of Health Science, and.
  • Akita N; Department of Clinical Engineering, Faculty of Medical Engineering, Suzuka University of Medical Science, Suzuka, Japan.
  • Hayashi T; Department of Biochemistry, Mie Prefectural College of Nursing, Tsu, Japan; and.
  • Suzuki K; Department of Molecular Pathobiology, Faculty of Pharmaceutical Sciences, Suzuka University of Medical Science, Suzuka, Japan.
  • Moriuchi H; Department of Pediatrics, Nagasaki University Hospital, Nagasaki, Japan.
Blood Adv ; 4(12): 2631-2639, 2020 06 23.
Article en En | MEDLINE | ID: mdl-32556284

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carboxipeptidasa B2 Límite: Humans Idioma: En Revista: Blood Adv Año: 2020 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carboxipeptidasa B2 Límite: Humans Idioma: En Revista: Blood Adv Año: 2020 Tipo del documento: Article País de afiliación: Japón