Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice

CaV2.1 Ca2+ channels play a key role in triggering neurotransmitter release and mediating synaptic transmission. 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) tr...

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Autores principales: Inchauspe, C.G., Pilati, N., Di Guilmi, M.N., Urbano, F.J., Ferrari, M.D., van den Maagdenberg, A.M.J.M., Forsythe, I.D., Uchitel, O.D.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03785955_v319_n_p56_Inchauspe
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