Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis (2020)
Source: Journal of Human Genetics. Unidade: FMRP
Subjects: AMILOIDOSE, GENÉTICA, FISIOPATOLOGIA, CARDIOPATIAS, MUTAÇÃO, LINHAGEM CELULAR
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SILVA-BATISTA, Jemima A. da et al. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis. Journal of Human Genetics, v. 65, n. 8, p. 711-713, 2020Tradução . . Disponível em: https://doi.org/10.1038/s10038-020-0749-3. Acesso em: 11 out. 2024.APA
Silva-Batista, J. A. da, Marques Júnior, W., Oliveira, M. T. de J. S., Lins, L. V. C., Galvão, A. J. P., Miguel, D. S. C. G., & Machado-Costa, M. C. (2020). Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis. Journal of Human Genetics, 65( 8), 711-713. doi:10.1038/s10038-020-0749-3NLM
Silva-Batista JA da, Marques Júnior W, Oliveira MT de JS, Lins LVC, Galvão AJP, Miguel DSCG, Machado-Costa MC. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis [Internet]. Journal of Human Genetics. 2020 ; 65( 8): 711-713.[citado 2024 out. 11 ] Available from: https://doi.org/10.1038/s10038-020-0749-3Vancouver
Silva-Batista JA da, Marques Júnior W, Oliveira MT de JS, Lins LVC, Galvão AJP, Miguel DSCG, Machado-Costa MC. Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis [Internet]. Journal of Human Genetics. 2020 ; 65( 8): 711-713.[citado 2024 out. 11 ] Available from: https://doi.org/10.1038/s10038-020-0749-3