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Autosomal dominant macrothrombocytopenia caused by a rare GPIBB variant: The importance of DNA sequencing.
De Kesel, Pieter M; Vantilborgh, Anna; Dierick, Jan; Luyckx, Ariane; Debussche, Sarah; Freson, Kathleen; Devreese, Katrien M J.
Afiliação
  • De Kesel PM; Department of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Vantilborgh A; Department of Hematology, Ghent University Hospital, Ghent, Belgium.
  • Dierick J; Department of Laboratory Medicine, AZ Maria Middelares, Ghent, Belgium.
  • Luyckx A; Department of Laboratory Medicine, AZ Maria Middelares, Ghent, Belgium.
  • Debussche S; Department of Hematology, AZ Maria Middelares, Ghent, Belgium.
  • Freson K; Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.
  • Devreese KMJ; Department of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium.
Int J Lab Hematol ; 42(3): e98-e100, 2020 06.
Article em En | MEDLINE | ID: mdl-31793234
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Plaquetários Limite: Humans Idioma: En Ano de publicação: 2020 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 Plaquetários Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article