Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations

M. Borhany, H. Handrkova, A. Cairo, V. Schroeder, N. Fatima, A. Naz, S. Amanat, T. Shamsi, F. Peyvandi, H. P. Kohler
  • Haemophilia, December 2013, Wiley
  • DOI: 10.1111/hae.12340
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The following have contributed to this page: Dr Munira Borhany