ISTH mutations

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Exon No	Alleles	VWD Classification	Nucleotide Change	Amino Acid Substitution	Functional Studies	Country	Laboratory	Comments	Ref.
15	200	Type 1	1781C>G	A594G	No	Spain	Vidal	VWF:Ag 37%, VWF:RCo 38%, FVIII:C 63%, ABO A blood group.	Corrales et al., 2009