APA (7th ed.) Citation

W, L., J, S., J, L., J, L., C, H., Y, L., . . . Y, F. (2018). ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss. Human genetics, 137(4), 329. https://doi.org/10.1007/s00439-018-1885-0

Chicago Style (17th ed.) Citation

W, Li, et al. "ELMOD3, a Novel Causative Gene, Associated with Human Autosomal Dominant Nonsyndromic and Progressive Hearing Loss." Human Genetics 137, no. 4 (2018): 329. https://doi.org/10.1007/s00439-018-1885-0.

MLA (9th ed.) Citation

W, Li, et al. "ELMOD3, a Novel Causative Gene, Associated with Human Autosomal Dominant Nonsyndromic and Progressive Hearing Loss." Human Genetics, vol. 137, no. 4, 2018, p. 329, https://doi.org/10.1007/s00439-018-1885-0.