Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hemophilia A and LCT[original query] |
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Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients. Blood 2016 Jun 127 (23): 2924-33. Gorski Marcin M, Blighe Kevin, Lotta Luca A, Pappalardo Emanuela, Garagiola Isabella, Mancini Ilaria, Mancuso Maria Elisa, Fasulo Maria Rosaria, Santagostino Elena, Peyvandi Flo |
Investigating the influence of LCT rs3754689 polymorphism on inhibitor development in Iranian and Afghan patients with severe hemophilia A. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2019 Oct . Bahrami Zadegan Sobhan, Mousavi Sayed H, Damavandi Narges, Samiee Aref Mohammad H, Zeinali Siro |
Influence of LCT rs3754689 polymorphism on inhibitor development in patients with severe hemophilia A. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2020 1 31 (1): 111. Mungmuunpuntipantip Rujittka, Wiwanitkit Vir |
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