Why patients with THBD c.1611C>A (p.Cys537X) nonsense mutation have high levels of soluble thrombomodulin?
Yohann Jourdy(Université Claude Bernard Lyon 1), Yesim Dargaud(Université Claude Bernard Lyon 1), Sandra Le Quellec(Hospices Civils de Lyon), Nathalie Enjolras(Université Claude Bernard Lyon 1), Christine Vinciguerra(Université Claude Bernard Lyon 1), Jean‐Claude Bordet(Hôpital Edouard Herriot), Claude Négrier(Unknown)
Cited by 11
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
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
|Blood|2020|60
Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization
|The American Journal of Human Genetics|2018|29
Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability
|Arteriosclerosis Thrombosis and Vascular Biology|2018|27