The expanded candidate interval included C1orf127 (chromosome 1 open reading frame 127), TARDBP (TAR DNA binding protein), MASP2 (mannan-binding lectin serine peptidase 2), SRM (spermidine synthase), EXOSC10 (exosome component 10), FRAP1 (FK506 binding protein 12-rapamycin associated protein 1), ANGPTL7 (angiopoietin-like 7), UBIAD1, and LOC39906. Recently, Orr and coworkers [9] reported that mutations in the UBIAD1 gene resulted in SCCD. The gene discussed is SRM; the disease is Schnyder corneal dystrophy.