F. Lehman-Horn

Synaptopathies Heat Up: Mutations in STX1B in Fever-Associated Epilepsies

L. Hood, R. Balling, F. Rüschendorf, 2015 .

Myopathy as the first symptom of hypokalemic periodic paralysis--case report of a girl from a Polish family with CACNA1S (R1239G) mutation.

K. Jurkat-Rott, B. Steinborn, B. Gurda, 2007, Advances in medical sciences.

Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family.

F. Incecik, M. O. Hergüner, Ş. Altunbaşak, 2010, The Turkish journal of pediatrics.