Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? (2010)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; BACHEGA, TÂNIA APARECIDA SARTORI SANCHEZ - FM
- Unidade: FM
- Subjects: FENÓTIPOS (VARIABILIDADE); HIDROXILASE (DEFICIÊNCIA); ALELOPATIA; GENÓTIPOS (VARIABILIDADE); TRANSTORNOS DA MENSTRUAÇÃO; PUBERDADE PRECOCE; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Simpósio "Avanços em Pesquisas Médicas dos Laboratórios de Investigação Médica do Hospital das Clínicas da FMUSP"
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ABNT
MOURA, V O et al. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency?. Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 21 fev. 2026. , 2010 -
APA
Moura, V. O., Pacheco, M., Madureira, G., Marcondes, J. A. M., Mendonça, B. B. de, & Bachega, T. A. S. S. (2010). Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Moura VO, Pacheco M, Madureira G, Marcondes JAM, Mendonça BB de, Bachega TASS. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. 2010 ; 65 S70.[citado 2026 fev. 21 ] -
Vancouver
Moura VO, Pacheco M, Madureira G, Marcondes JAM, Mendonça BB de, Bachega TASS. Could genetic variants in the CYP2C19, CYP3A4, CYP3A5, CYP17, CYP3A7 genes contribute for the phenotypic variability of nonclassical 21-hydroxylase deficiency? Clinics. 2010 ; 65 S70.[citado 2026 fev. 21 ] - Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency
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