TURKISH JOURNAL OF PEDIATRICS, cilt.52, sa.4, ss.409-410, 2010 (SCI-Expanded)
Incecik F, Herguner MO, Altunbasak S, Lehman-Horn F. Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family. Turk J Pediatr 2010; 52: 409-410.