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

Research output: Contribution to journalArticlepeer-review

Fingerprint

Dive into the research topics of 'Congenital factor XIII deficiency in Pakistan: Characterization of seven families and identification of four novel mutations'. Together they form a unique fingerprint.

Medicine & Life Sciences