Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes

MLA

Caio Robledo D’ Angioli Costa Quaio, et al. “Genomic Study of Nonsyndromic Hearing Loss in Unaffected Individuals: Frequency of Pathogenic and Likely Pathogenic Variants in a Brazilian Cohort of 2,097 Genomes.” Frontiers in Genetics, vol. 13, Aug. 2022. EBSCOhost, https://doi.org/10.3389/fgene.2022.921324.

APA

Caio Robledo D’ Angioli Costa Quaio, Antonio Victor Campos Coelho, Livia Maria Silva Moura, Rafael Lucas Muniz Guedes, Kelin Chen, Jose Ricardo Magliocco Ceroni, Renata Moldenhauer Minillo, Marcel Pinheiro Caraciolo, Rodrigo de Souza Reis, Bruna Mascaro Cordeiro de Azevedo, Maria Soares Nobrega, Anne Caroline Barbosa Teixeira, Matheus Martinelli Lima, Thamara Rayssa da Mota, Marina Cadena da Matta, Gabriela Borges Cherulli Colichio, Aline Lulho Roncalho, Ana Flavia Martinho Ferreira, Gabriela Pereira Campilongo, … Joao Bosco de Oliveira Filho. (2022). Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.921324

Chicago

Caio Robledo D’ Angioli Costa Quaio, Antonio Victor Campos Coelho, Livia Maria Silva Moura, Rafael Lucas Muniz Guedes, Kelin Chen, Jose Ricardo Magliocco Ceroni, Renata Moldenhauer Minillo, et al. 2022. “Genomic Study of Nonsyndromic Hearing Loss in Unaffected Individuals: Frequency of Pathogenic and Likely Pathogenic Variants in a Brazilian Cohort of 2,097 Genomes.” Frontiers in Genetics 13 (August). doi:10.3389/fgene.2022.921324.