Lezirovitz, K., Vieira-Silva, G. A., Batissoco, A. C., Levy, D., Kitajima, J. P., Trouillet, A., . . . Oiticica, J. (2020). A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Hum Mol Genet.
Chicago Style CitationLezirovitz, Karina, et al. "A Rare Genomic Duplication in 2p14 Underlies Autosomal Dominant Hearing Loss DFNA58." Hum Mol Genet 2020.
MLA CitationLezirovitz, Karina, et al. "A Rare Genomic Duplication in 2p14 Underlies Autosomal Dominant Hearing Loss DFNA58." Hum Mol Genet 2020.
Warning: These citations may not always be 100% accurate.