Fonte: Human Genome Variation. Unidades: IB, FM
Assuntos: MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA, PERDA AUDITIVA, SURDEZ, DELEÇÃO DE GENES, DOENÇAS GENÉTICAS, DOENÇAS HEREDITÁRIAS
ABNT
UEHARA, Daniela T et al. A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. Human Genome Variation, v. 2, 2015Tradução . . Disponível em: https://doi.org/10.1038/hgv.2015.38. Acesso em: 26 ago. 2024.APA
Uehara, D. T., Freitas, E. L., Alves, L. U., Mazzeu, J. F., Auricchio, M. T. B. de M., Tabith Jr, A., et al. (2015). A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. Human Genome Variation, 2. doi:10.1038/hgv.2015.38NLM
Uehara DT, Freitas EL, Alves LU, Mazzeu JF, Auricchio MTB de M, Tabith Jr A, Monteiro MLM, Rosenberg C, Mingroni Netto RC. A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family [Internet]. Human Genome Variation. 2015 ; 2[citado 2024 ago. 26 ] Available from: https://doi.org/10.1038/hgv.2015.38Vancouver
Uehara DT, Freitas EL, Alves LU, Mazzeu JF, Auricchio MTB de M, Tabith Jr A, Monteiro MLM, Rosenberg C, Mingroni Netto RC. A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family [Internet]. Human Genome Variation. 2015 ; 2[citado 2024 ago. 26 ] Available from: https://doi.org/10.1038/hgv.2015.38