Clinical, molecular, functional, and structural characterization of CYP17A1 mutations in brazilian patients with 17-hydroxylase deficiency (2020)
- Authors:
- USP affiliated authors: LACCHINI, FERNANDA BORCHERS COELI - FMRP ; ELIAS, LUCILA LEICO KAGOHARA - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; ANTONINI, SONIR ROBERTO RAUBER - FMRP ; MOREIRA, AYRTON CUSTODIO - FMRP ; CASTRO, MARGARET DE - FMRP ; BODONI, ALINE FACCIOLI - FMRP
- Unidade: FMRP
- DOI: 10.1055/a-1100-7066
- Subjects: HIPERPLASIAS; SEQUÊNCIA DE AMINOÁCIDOS; SEQUÊNCIA DE BASES; HORMÔNIOS; ESTEROIDES
- Keywords: CAH; CYP17A1 gene; 17OH deficiency; Molecular structure
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Hormone and Metabolic Research
- ISSN: 0018-5043
- Volume/Número/Paginação/Ano: v. 52, n. 3, p. 186-193, 2020
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
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: 25 jan. 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-1100-7066 -
NLM
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 jan. 25 ] Available from: https://doi.org/10.1055/a-1100-7066 -
Vancouver
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 jan. 25 ] Available from: https://doi.org/10.1055/a-1100-7066 - Loss-of-function NNT mutations impair antioxidantes mechanisms and decreases cortisol secretion in patients with famililar glucocorticoid deficiency
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Informações sobre o DOI: 10.1055/a-1100-7066 (Fonte: oaDOI API)
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