Suleimanova A.; Talanov M.; van den Maagdenberg A.M.J.M.; Giniatullin R.
(2021)
Familial hemiplegic migraine type 3 (FHM3) is caused by gain-of-function mutations in the SCN1A gene that encodes the α1 subunit of voltage-gated NaV1.1 sodium channels. The high level of expression of NaV1.1 channels in ...