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Autor:
Alla Zozulya Weidenfeller, Laure Weijers, M. Schurer, Crispin Ellis, Hiba Lee, A.M. Chapman, Shaneil Sonecha, Christiane Schneider-Gold, Amer Omar
Publikováno v:
BMC Neurology
BMC Neurology, Vol 21, Iss 1, Pp 1-16 (2021)
BMC Neurology, Vol 21, Iss 1, Pp 1-16 (2021)
Background Non-dystrophic myotonias (NDMs) comprise muscle chloride and sodium channelopathies due to genetic defects of the CLCN1- and SCN4A-channels. No licensed antimyotonic treatment has been available until approval of mexiletine (NaMuscla®) fo