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Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance
Plassart-Schiess, E., Gervais, A., Eymard, B., Lagueny, A., Pouget, J., Warter, J. M., Fardeau, M., Jentsch, T. J., Fontaine, B.Volume:
50
Language:
english
Journal:
Neurology
DOI:
10.1212/WNL.50.4.1176
Date:
April, 1998
File:
PDF, 469 KB
english, 1998