APA (7th ed.) Citation

Coutelier, M., Blesneac, I., Monteil, A., Monin, M., Ando, K., Mundwiller, E., . . . Stevanin, G. (2015). A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia. American journal of human genetics, 97(5), 726-737. https://doi.org/10.1016/j.ajhg.2015.09.007

Chicago Style (17th ed.) Citation

Coutelier, Marie, et al. "A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia." American Journal of Human Genetics 97, no. 5 (2015): 726-737. https://doi.org/10.1016/j.ajhg.2015.09.007.

MLA (9th ed.) Citation

Coutelier, Marie, et al. "A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia." American Journal of Human Genetics, vol. 97, no. 5, 2015, pp. 726-737, https://doi.org/10.1016/j.ajhg.2015.09.007.