APA (7th ed.) Citation

H, G., CB, E., FD, C., MJ, M., KD, Z., CD, L., . . . CL, R. (2018). TMTC2 variant associated with sensorineural hearing loss and auditory neuropathy spectrum disorder in a family dyad. Molecular genetics & genomic medicine, 6(4), 653. https://doi.org/10.1002/mgg3.397

Chicago Style (17th ed.) Citation

H, Guillen-Ahlers, Erbe CB, Chevalier FD, Montoya MJ, Zimmerman KD, Langefeld CD, Olivier M, and Runge CL. "TMTC2 Variant Associated with Sensorineural Hearing Loss and Auditory Neuropathy Spectrum Disorder in a Family Dyad." Molecular Genetics & Genomic Medicine 6, no. 4 (2018): 653. https://doi.org/10.1002/mgg3.397.

MLA (9th ed.) Citation

H, Guillen-Ahlers, et al. "TMTC2 Variant Associated with Sensorineural Hearing Loss and Auditory Neuropathy Spectrum Disorder in a Family Dyad." Molecular Genetics & Genomic Medicine, vol. 6, no. 4, 2018, p. 653, https://doi.org/10.1002/mgg3.397.