Targeted Next-Generation Resequencing of Gene Identifies Novel Multiple Variants Pattern in Severe Hereditary Factor V Deficiency
Figure 1
Segregation of missense variants 2102 R/H (exon 23), 513 R/K (exon 10) and 107 D/H (exon 3). Half-filled symbols indicate heterozygotes for investigated mutatons. Completely filled symbols indicate homozygous for all investigated mutations (i.e., proband). Open symbols indicate no carrier of investigated mutations. Question marks indicate that genotyping has not been performed.
