Clonal iPSC lines were derived from two variant late infantile BD patients; a female diagnosed at 2.5 years and genotyped with homozygous CLN7 c.881 C > A (p.T294K, hereafter referred to as BD1) and a male diagnosed at 4.5 years genotyped with homozygous CLN7 c.1393 C > T (R465W, hereafter referred to as BD2) (Table 1). This evidence concerns the gene MFSD8 and Behcet disease.