Multiple alignment of genomic DNA sequence surrounding the putative stop codon mutation within the Kindlin3 F3 region. The reference genome (NCBI human genome database build 36.2, chr11: 63744678-63744716), the mRNA (RefSeq: NM_178443.1), and genomic sequences from one normal control, one parent of a LADIII patient (LAD-A), and 3 LADIII patients (LAD-A, LAD-K, and LAD-N) were aligned surrounding the mutation nt1632c > t. The base of the mutation is highlighted.