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 Stili AlıntıDoll, Julia, Michaela A. H. Hofrichter, Paulina Bahena, Alfred Heihoff, Dennis Segebarth, Tobias Müller, Marcus Dittrich, Thomas Haaf, ve 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.
MLA AlıntıDoll, 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.