Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation

por Thor, Michael G., Vivekanandam, Vinojini, Sampedro-Castañeda, Marisol, Tan, S. Veronica, Suetterlin, Karen, Sud, Richa, Durran, Siobhan, Schorge, Stephanie, Kullmann, Dimitri M., Hanna, Michael G., Matthews, Emma, Männikkö, Roope
Publicado 2019