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Autor:
Alin Pȋnzariu, Maria Vladeanu, Oana Viola Badulescu, Iris Bararu-Bojan, Carmen Ungureanu, Manuela Ciocoiu, Paul Dan Sirbu, Elena Cojocaru, Nina Filip
Publikováno v:
Exp Ther Med
Hemophilia is a hereditary coagulopathy caused by factor VIII (hemophilia type A) or by coagulation factor IX (hemophilia type B) dysfunction, characterized by an increased bleeding predisposition, which is either spontaneous or secondary to minimal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::921f217d45093dbe263d88d0a327ba9e
https://doi.org/10.3892/etm.2021.10427
https://doi.org/10.3892/etm.2021.10427
