Cita APA

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. Mol Genet Genomic Med.

Chicago Style Citation

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

Cita MLA

Doll, Julia, et al. "A Novel Missense Variant in MYO3A Is Associated With Autosomal Dominant High‐frequency Hearing Loss in a German Family." Mol Genet Genomic Med 2020.