Article
Enzymes that hydrolyze adenine nucleotides in platelets and polymorphisms in the alpha2 gene of integrin alpha2beta1 in patients with von Willebrand disease.
Molecular and cellular biochemistry - 1 Jul 2010
Santos Karen Freitas, Battisti Vanessa, Corrêa Maísa de Carvalho, Mann Thaís Rapachi, Pereira Renata da Silva, Araújo Maria do Carmo, Brülê Alice Odete, Schetinger Maria Rosa Chitolina, Morsch Vera Maria
Abstract excerpt
Von Willebrand disease (VWD) is one of the most common inherited bleeding diseases caused by a qualitative or quantitative deficiency of the von Willebrand factor (FvW). FvW is a multimeric glycoprotein synthesized by megakaryocytes and endothelial cells and it is present in the subendothelial ma...
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