Dias, Alex Marcel Moreira; Lezirovitz, Karina 
; Nicastro, Fernanda Stávale; Mendes, Beatriz C. A; Mingroni Netto, Regina Celia
Fonte: Journal of Human Genetics. Unidade: IB
Assuntos: PERDA AUDITIVA, SURDEZ, SEQUENCIAMENTO GENÉTICO, ACONSELHAMENTO GENÉTICO, MUTAÇÃO GENÉTICA
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ABNT
DIAS, Alex Marcel Moreira et al. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of Human Genetics, v. 64, p. 257–260, 2019Tradução . . Disponível em: https://doi.org/10.1038/s10038-018-0546-4. Acesso em: 16 ago. 2024.APA
Dias, A. M. M., Lezirovitz, K., Nicastro, F. S., Mendes, B. C. A., & Mingroni Netto, R. C. (2019). Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. Journal of Human Genetics, 64, 257–260. doi:10.1038/s10038-018-0546-4NLM
Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans [Internet]. Journal of Human Genetics. 2019 ; 64 257–260.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1038/s10038-018-0546-4Vancouver
Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni Netto RC. Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans [Internet]. Journal of Human Genetics. 2019 ; 64 257–260.[citado 2024 ago. 16 ] Available from: https://doi.org/10.1038/s10038-018-0546-4
