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


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

HAEMOPHILIA, vol.16, no.2, pp.408, 2010 (Peer-Reviewed Journal) identifier

  • Publication Type: Article / Abstract
  • Volume: 16 Issue: 2
  • Publication Date: 2010
  • Journal Name: HAEMOPHILIA
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.408