| 1 | CACNA1G, SCA42 |
| A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia. | |
| Coutelier M, Blesneac I, Monteil A, Monin ML, Ando K, Mundwiller E, Brusco A, Le Ber I, Anheim M, Castrioto A, Duyckaerts C, Brice A, Durr A, Lory P, Stevanin G. | |
| Am J Hum Genet 97(5):726-37. doi: 10.1016/j.ajhg.2015.09.007. Epub 2015 Oct 8. 2015 | |