Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization
Yohann Jourdy(Université Claude Bernard Lyon 1), Christine Vinciguerra(Université Claude Bernard Lyon 1), Anne Lienhart(Lille’s Cardiology Hospital), Claude Négrier(Unknown), Dominique Bozon(Hospices Civils de Lyon), Alexandre Janin(Université Claude Bernard Lyon 1), Mathilde Frétigny(Hospices Civils de Lyon)
Cited by 29
Related Papers
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families.
|PubMed|1999|92
Utilization of Previously Treated Patients (PTPs), Noninfected Patients (NIPs), and Previously Untreated Patients (PUPs) in the Evaluation of New Factor VIII and Factor IX Concentrates
|Thrombosis and Haemostasis|1999|61
Splicing analysis of 26 <i>F8</i> nucleotide variations using a minigene assay
|Haemophilia|2019|17
Severe hemophilia A caused by an unbalanced chromosomal rearrangement identified using nanopore sequencing
|Journal of Thrombosis and Haemostasis|2019|15