A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia
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author: Marie Coutelier, Arnaud Monteil, Kunie Ando, Alfredo Brusco, Mathieu Anheim, Alexis Brice, Philippe Lory, Giovanni Stevanin, Alexandra Durr, Emeline Mundwiller, Marie-Lorraine Monin, Isabelle Le Ber, Charles Duyckaerts, Anna Castrioto
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