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Among calcium channel mutations, CACNA1H, a T-type calcium channel subunit called Ca v 3.2, has shown three missense mutations in patients with genetic generalized epilepsy and has displayed enhanced channel function [48,49]

JAMA Oncol 4:930937 Doti N, Mardirossian M, Sandomenico A, Ruvo M, Caporale A (2021) Recent applications of retro-inverso peptides

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