Coexistence of CLCN1 and SCN4A mutations in one family suffering from myotonia.Published in:Neurogenetics, 2017, v. 18, n. 4, p. 219, doi. 10.1007/s10048-017-0525-5By:Maggi, Lorenzo;Ravaglia, Sabrina;Farinato, Alessandro;Brugnoni, Raffaella;Altamura, Concetta;Imbrici, Paola;Camerino, Diana;Padovani, Alessandro;Mantegazza, Renato;Bernasconi, Pia;Desaphy, Jean-François;Filosto, MassimilianoPublication type:Article