Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon

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Aytac S., ÜNAL S., Coskun T., Tokatli A., Sivri S., DURSUN A., ...More

HAEMOPHILIA, vol.16, no.2, pp.408, 2010 (SCI-Expanded)

• Publication Type: Article / Abstract
• Volume: 16 Issue: 2
• Publication Date: 2010
• Journal Name: HAEMOPHILIA
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.408
• Hacettepe University Affiliated: Yes