Description
No F8 genetic abnormality is detected in about 1-2% of patients with severe haemophilia A using conventional genetic approaches. In these patients, deep intronic variation or F8 disrupting genomic rearrangement could be causal.
Journal of thrombosis and haemostasis : JTH Mar 2024
No F8 genetic abnormality is detected in about 1-2% of patients with severe haemophilia A using conventional genetic approaches. In these patients, deep intronic variation or F8 disrupting genomic rearrangement could be causal.