APA (7th ed.) Citation

Doll, J., Hofrichter, M. A. H., Bahena, P., Heihoff, A., Segebarth, D., Müller, T., . . . Vona, B. (2020). A novel missense variant in MYO3A is associated with autosomal dominant high‐frequency hearing loss in a German family. Wiley.

Chicago Style (17th ed.) Citation

Doll, Julia, Michaela A. H. Hofrichter, Paulina Bahena, Alfred Heihoff, Dennis Segebarth, Tobias Müller, Marcus Dittrich, Thomas Haaf, and Barbara Vona. A Novel Missense Variant in MYO3A Is Associated with Autosomal Dominant High‐frequency Hearing Loss in a German Family. Wiley, 2020.

MLA (9th ed.) Citation

Doll, Julia, et al. A Novel Missense Variant in MYO3A Is Associated with Autosomal Dominant High‐frequency Hearing Loss in a German Family. Wiley, 2020.