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Items for "VWF mRNA"

Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease

We describe the complex picture associated with a mutated splice junction in intron 13 of von Willebrand factor (VWF) gene...

Keywords: von Willebrand factor, von Willebrand disease, VWF mRNA, VWF mutations

12/2006 | Thrombosis and Haemostasis, Schattauer