Associated Papers
A novel splicing mutation in F8 causes various aberrant transcripts in a hemophilia A patient and identifies a new transcript from healthy individuals.
Yi S et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2020
Splicing analysis of 26 F8 nucleotide variations using a minigene assay.
Jourdy Y et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2019
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