Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine

por De Vries, B, Weller, CM, De Fàbregues, O, Koelewijn, SC, Stam, AH, Haan, J, Ferrari, MD, Terwindt, GM, van den Maagdenberg, AMJ
Publicado 2013