APA Alıntı

Houle, G., Ambalavanan, A., Schmouth, J., Leblond, C. S., Spiegelman, D., Laurent, S. B., . . . Rouleau, G. A. (2017). No rare deleterious variants from STK32B, PPARGC1A, and CTNNA3 are associated with essential tremor. Neurol Genet.

Chicago Stili Alıntı

Houle, Gabrielle, et al. "No Rare Deleterious Variants From STK32B, PPARGC1A, and CTNNA3 Are Associated With Essential Tremor." Neurol Genet 2017.

MLA Alıntı

Houle, Gabrielle, et al. "No Rare Deleterious Variants From STK32B, PPARGC1A, and CTNNA3 Are Associated With Essential Tremor." Neurol Genet 2017.