Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.

CONCLUSIONS: In Iran, with its high rate of consanguinity, autosomal recessive afibrinogenemia with severe clinical presentations is relatively common due to heterogeneous molecular defects.
PMID: 32639687 [PubMed - as supplied by publisher]

Source: International Journal of Laboratory Hematology - July 7, 2020 Category: Hematology Authors: Tavasoli B, Safa M, Dorgalaleh A, Ghasemi JB, Rezaei Makhouri F, Rezvani MR, Ahmadi A, Tabibian S, Jazebi M, Baghaipor MR, Zaker F Tags: Int J Lab Hematol Source Type: research