Olgu Sunumu: Ağır Trombositopenili Bir Bebekte De Novo p.Val1316Met Mutasyonuna Bağlı Von Willebrand Hastalığı Tip 2B Tanısı
Junjie Fan, Jing Ling, Huifeng Zhou, Jie He, Shaoyan HuChildren’s Hospital of Soochow University, Department of Hematology and Oncology, Jiangsu, ChinaAnahtar Kelimeler: Von Willebrand Hastalığı Tip2B, VWF geni, Trombositopeni
Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation
Junjie Fan, Jing Ling, Huifeng Zhou, Jie He, Shaoyan HuChildren’s Hospital of Soochow University, Department of Hematology and Oncology, Jiangsu, ChinaKeywords: Type 2B von Willebrand disease, VWF gene, Thrombocytopenia
Junjie Fan, Jing Ling, Huifeng Zhou, Jie He, Shaoyan Hu. Case Report: An Infant with Severe Thrombocytopenia Diagnosed with Type 2B von Willebrand Disease Due To a De Novo p.Val1316Met Mutation. . 2020; 37(4): 296-298
Sorumlu Yazar: Shaoyan Hu, Saint Kitts and Nevis
Sorumlu Yazar: Shaoyan Hu, Saint Kitts and Nevis
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