ISTH mutations

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Exon No	Alleles	VWD Classification	Nucleotide Change	Amino Acid Substitution	Functional Studies	Country	Laboratory	Comments	Ref.
28	200	Type 2A	3835G>T	V1279F	No	Spain	Vidal	VWF:Ag 24%, VWF:RCo 10%, FVIII:C 48%, ABO A blood group.	Corrales et al., 2009