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Purpura fulminans in a child with combined heterozygous prothrombin G20210A and factor V Leiden mutations

✍ Scribed by N. Özbek; F. B. Ataç; H. Verdi; S. M. Kayıran

Publisher: Springer
Year: 2003
Tongue: English
Weight: 92 KB
Volume: 82
Category: Article
ISSN: 0939-5555
DOI: 10.1007/s00277-003-0613-5

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## Objective: To evaluate the frequency and type of vascular lesions and to study the association of factor v gene g1691a (leiden) and prothrombin gene g20210a polymorphisms with venous thrombosis in italian patients with behçet's disease (bd). ## Methods: Included were 118 consecutive italian bd