Coeli-Lacchini, Fernanda Borchers 
; Mermejo, Livia M.; Bodoni, Aline Faccioli; Elias, Lucila Leico Kagohara ; Silva Junior, Wilson Araújo da ; Antonini, Sonir Roberto Rauber ; Moreira, Ayrton Custódio ; Castro, Margaret de
Source: Hormone and Metabolic Research. Unidade: FMRP
Subjects: HIPERPLASIAS, SEQUÊNCIA DE AMINOÁCIDOS, SEQUÊNCIA DE BASES, HORMÔNIOS, ESTEROIDES
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COELI-LACCHINI, Fernanda Borchers et al. Clinical, molecular, functional, and structural characterization of CYP17A1 mutations in brazilian patients with 17-hydroxylase deficiency. Hormone and Metabolic Research, v. 52, n. 3, p. 186-193, 2020Tradução . . Disponível em: https://doi.org/10.1055/a-1100-7066. Acesso em: 06 maio 2026.APA
Coeli-Lacchini, F. B., Mermejo, L. M., Bodoni, A. F., Elias, L. L. K., Silva Junior, W. A. da, Antonini, S. R. R., et al. (2020). Clinical, molecular, functional, and structural characterization of CYP17A1 mutations in brazilian patients with 17-hydroxylase deficiency. Hormone and Metabolic Research, 52( 3), 186-193. doi:10.1055/a-1100-7066NLM
Coeli-Lacchini FB, Mermejo LM, Bodoni AF, Elias LLK, Silva Junior WA da, Antonini SRR, Moreira AC, Castro M de. Clinical, molecular, functional, and structural characterization of CYP17A1 mutations in brazilian patients with 17-hydroxylase deficiency [Internet]. Hormone and Metabolic Research. 2020 ; 52( 3): 186-193.[citado 2026 maio 06 ] Available from: https://doi.org/10.1055/a-1100-7066Vancouver
Coeli-Lacchini FB, Mermejo LM, Bodoni AF, Elias LLK, Silva Junior WA da, Antonini SRR, Moreira AC, Castro M de. Clinical, molecular, functional, and structural characterization of CYP17A1 mutations in brazilian patients with 17-hydroxylase deficiency [Internet]. Hormone and Metabolic Research. 2020 ; 52( 3): 186-193.[citado 2026 maio 06 ] Available from: https://doi.org/10.1055/a-1100-7066
