학술논문
Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes
Document Type
Article
Author
Quaio, C.R.D.A.C.; Coelho, A.V.C.; Moura, L.M.S.; Guedes, R.L.M.; Chen, K.; Ceroni, J.R.M.; Minillo, R.M.; Caraciolo, M.P.; Reis, R.D.S.; Azevedo, B.M.C.D.; Nobrega, M.S.; Teixeira, A.C.B.; Martinelli Lima, M.; Mota, T.R.D.; Matta, M.C.D.; Colichio, G.B.C.; Roncalho, A.L.; Ferreira, A.F.M.; Campilongo, G.P.; Perrone, E.; Virmond, L.D.A.; Moreno, C.A.; Prota, J.R.M.; França, M.D.; Cervato, M.C.; Almeida, T.F.D.; Oliveira Filho, J.B.D.
Source
In: Frontiers in Genetics . (Frontiers in Genetics, 30 August 2022, 13)
Subject
Language
English
ISSN
16648021