ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype–phenotype correlation

Por Imbrici, P, Maggi, L, Mangiatordi, G F, Dinardo, M M, Altamura, C, Brugnoni, R, Alberga, D, Pinter, G Lauria, Ricci, G, Siciliano, G, Micheli, R, Annicchiarico, G, Lattanzi, G, Nicolotti, O, Morandi, L, Bernasconi, P, Desaphy, J-F, Mantegazza, R, Camerino, D Conte
Publicado no J Physiol (2015)