These genes were LRRC6 [MIM:614930], DNAH11 [MIM:603339], DNAAF1 [MIM:613190], CCDC114 [MIM:615038], and DNAH5 [MIM: 603335] (the latter mutated in two SI cases with PCD, consistent with DNAH5 being the most common cause of PCD in European-ancestry populations62) (Table 1). The gene discussed is ODAD1; the disease is primary ciliary dyskinesia.