ISTH mutations

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Exon No	Alleles	VWD Classification	Nucleotide Change	Amino Acid Substitution	Functional Studies	Country	Laboratory	Comments	Ref.
28	12	Type 1	3944G>A	R1315H	No	EU	MCMDM-1VWD	Mutation associated with an abnormal multimer pattern.	Goodeve et al., 2007