File S1 - Genetic Heterogeneity in a Large Cohort of Indian Type 3 von Willebrand Disease Patients

Tables S1–S3. Table S1: Primer sequence for screening known Arginine hot spot regions of VWF. Blue coloured font indicates artificial restriction site has been introduced by using a mismatched nucleotide. The bold font in the oligonucleotides represents a mismatched nucleotide. Table S2: Mutation detection by PCR-RFLP for Arginine hot spot mutations. R- arginine, *- stop codon. Adapted from Baronciani et al., 2000. Table S3: Primers used for sequencing are shown in table. (DOC)