In 28 of these 29 infants, a molecular screening for mutations in any of the LQTS genes KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, CAV3, and SCN4B, associated with the LQTS types 1–3, 5, 6, 9, and 10, respectively (Table 1), was performed. The gene discussed is KCNE2; the disease is familial long QT syndrome.