Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N
Dokumenttyp:
Journal Article
Autor(en):
Berber, E.; Fidanci, I. D.; Un, C.; El-Maarri, O.; Aktuglu, G.; Gurgey, A.; Celkan, T.; Meral, A.; Oldenburg, J.; Graw, J.; Akar, N.; Caglayan, H.