APA Цитирование

Smits, J. J., Oostrik, J., Beynon, A. J., Kant, S. G., de Koning Gans, P. A. M., Rotteveel, L. J. C., . . . Kremer, H. (2018). De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. Hum Genet.

Chicago-стиль цитирования

Smits, Jeroen J., et al. "De Novo and Inherited Loss-of-function Variants of ATP2B2 Are Associated With Rapidly Progressive Hearing Impairment." Hum Genet 2018.

MLA-цитирование

Smits, Jeroen J., et al. "De Novo and Inherited Loss-of-function Variants of ATP2B2 Are Associated With Rapidly Progressive Hearing Impairment." Hum Genet 2018.

Предупреждение: эти цитированмия не могут быть всегда правильны на 100%.