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First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.
Nagaya, Satomi; Maruyama, Keiko; Watanabe, Atsushi; Meguro-Horike, Makiko; Imai, Yuta; Hiroshima, Yuki; Horike, Shin-Ichi; Kokame, Koichi; Morishita, Eriko.
Afiliação
  • Nagaya S; Department of Clinical Laboratory Science, Division of Health Sciences, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa.
  • Maruyama K; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Osaka.
  • Watanabe A; Division of Clinical Genetics, Kanazawa University Hospital, Kanazawa, Ishikawa.
  • Meguro-Horike M; Advanced Science Research Center, Kanazawa University, Kanazawa, Ishikawa.
  • Imai Y; Department of Clinical Laboratory Science, Division of Health Sciences, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa.
  • Hiroshima Y; Department of Hematology, Nagano Red Cross Hospital, Nagano, Nagano.
  • Horike SI; Advanced Science Research Center, Kanazawa University, Kanazawa, Ishikawa.
  • Kokame K; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Osaka.
  • Morishita E; Department of Clinical Laboratory Science, Division of Health Sciences, Graduate School of Medical Science, Kanazawa University, Kanazawa, Ishikawa, Japan; Department of Hematology, Kanazawa University Hospital, Kanazawa, Ishikawa. eriko86@staff.kanazawa-u.ac.jp.
Haematologica ; 107(1): 330-333, 2022 01 01.
Article em En | MEDLINE | ID: mdl-34647440
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Deficiência de Proteína S / Trombofilia Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Haematologica Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Deficiência de Proteína S / Trombofilia Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Haematologica Ano de publicação: 2022 Tipo de documento: Article