A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type...

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A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia

Coutelier, Marie, Blesneac, Iulia, Monteil, Arnaud, Monin, Marie-Lorraine, Ando, Kunie, Mundwiller, Emeline, Brusco, Alfredo, Le Ber, Isabelle, Anheim, Mathieu, Castrioto, Anna, Duyckaerts, Charles, B
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Language:
english
Journal:
The American Journal of Human Genetics
DOI:
10.1016/j.ajhg.2015.09.007
Date:
October, 2015
File:
PDF, 2.36 MB
english, 2015
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