Supplementary MaterialsDocument S1. sequencing dataset of 18 identical case topics and 1 phenotypically,917 control subjects. Using a recessive model and a binomial test for rare, presumed biallelic, variants, we found to be the most statistically enriched gene; one subject was a homozygote (c.362A T [p.His121Leu]) and another a compound heterozygote (c.79T C [p.Tyr27His] and c.217_225del… Continue reading Supplementary MaterialsDocument S1. sequencing dataset of 18 identical case topics and