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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." Mol Genet Genomic Med 2020.

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.