A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 (2020)
Lezirovitz, Karina; Vieira-silva, Gleiciele A; Batissoco, Ana C; Levy, Debora; Kitajima, Joao P; Trouillet, Alix; Ouyang, Ellen; Zebarjadi, Navid; Sampaio-Silva, Juliana; Bento, Ricardo Ferreira 
Source: Human molecular genetics. Unidade: FM
Subjects: GENES, PERDA AUDITIVA, SURDEZ, NEURÔNIOS
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LEZIROVITZ, Karina et al. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Human molecular genetics, v. 29, n. 9, p. 1520-1536, 2020Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddaa075. Acesso em: 17 nov. 2024.APA
Lezirovitz, K., Vieira-silva, G. A., Batissoco, A. C., Levy, D., Kitajima, J. P., Trouillet, A., et al. (2020). A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Human molecular genetics, 29( 9), 1520-1536. doi:10.1093/hmg/ddaa075NLM
Lezirovitz K, Vieira-silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Bento RF. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 [Internet]. Human molecular genetics. 2020 ; 29( 9): 1520-1536.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1093/hmg/ddaa075Vancouver
Lezirovitz K, Vieira-silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Bento RF. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 [Internet]. Human molecular genetics. 2020 ; 29( 9): 1520-1536.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1093/hmg/ddaa075
