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New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia.
Ferrari, Silvia; Lombardi, Anna M; Cortella, Irene; Businaro, Maria A; Bertomoro, Antonella; Di Pasquale, Irene; Fabris, Fabrizio.
Afiliação
  • Ferrari S; Department of Medicine, University of Padua Medical School, Padua, Italy.
  • Lombardi AM; Department of Medicine, University of Padua Medical School, Padua, Italy.
  • Cortella I; Department of Medicine, University of Padua Medical School, Padua, Italy.
  • Businaro MA; Department of Medicine, University of Padua Medical School, Padua, Italy.
  • Bertomoro A; Department of Medicine, University of Padua Medical School, Padua, Italy.
  • Di Pasquale I; Department of Medicine, University of Padua Medical School, Padua, Italy.
  • Fabris F; Department of Medicine, University of Padua Medical School, Padua, Italy.
Br J Haematol ; 184(5): 855-858, 2019 03.
Article em En | MEDLINE | ID: mdl-29527674
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bernard-Soulier / Complexo Glicoproteico GPIb-IX de Plaquetas / Heterozigoto / Mutação Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bernard-Soulier / Complexo Glicoproteico GPIb-IX de Plaquetas / Heterozigoto / Mutação Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article