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Autor:
Alexandra V. Serezhkina, Irina G. Khmelevskaya, Natalya S. Razinkova, Irina I. Zhiznevskaya, Tatyana A. Minenkova, Tatyana V. Feoktistova, Maxim P. Ivenkov
Publikováno v:
Клинический разбор в общей медицине, Vol 5, Iss 2, Pp 98-100 (2024)
Hemophilia B is a hereditary, X-linked recessive disease caused by a violation of plasma homeostasis, resulting from a deficiency or absence of coagulation factor IX (FIX). The cause is a mutation of the Xq27 gene encoding FIX. A serious complication
Externí odkaz:
https://doaj.org/article/e40caecc5a3344cb81a9fc9f31152d73
