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Gain of function in FHM-1 Cav2.1 knock-in mice is related to the shape of the action potential
(American Physiological Society, 2010-07)
Familial hemiplegic migraine type-1 FHM-1 is caused by missense mutations in the CACNA1A gene that encodes the α1A pore-forming subunit of CaV2.1 Ca2+ channels. We used knock-in (KI) transgenic mice harboring the pathogenic ...
Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models
(Springer Verlag Berlín, 2014)