Original article
Redefining periodic paralysis with CACNA1S mutation in a Spanish cohort
Redefiniendo la parálisis periódica por mutación en el gen CACNA1S en una cohorte española
P. Carbonell-Corvilloa,b,f, E. Rivasc, M. Cabreraa, A. García-Redondod, A. Fernándeze, C. Paradasa,
Corresponding author
a Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario Virgen del Rocío/Instituto de Biomedicina de Sevilla (IBiS)/CSIC/Universidad de Sevilla, Seville, Spain
b Department of Neurology, Hospital Universitario Virgen de la Victoria, Málaga, Spain
c Department of Neuropathology, Hospital Universitario Virgen del Rocío, Seville, Spain
d Neurology Department, ALS Unit, Biomedical Research Networking Center on Rare Diseases (CIBERER) U-723, Madrid, Spain
e Department of Social and Health Sciences, Universidad de Sevilla, Seville, Spain
f Instituto de Investigación Biomédica de Málaga (IBIMA), Málaga, Spain
