Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients (2009)
- Authors:
- USP affiliated authors: MENDONÇA, BERENICE BILHARINHO DE - FM ; CASTRO, MARGARET DE - FMRP
- Unidades: FM; FMRP
- Subjects: HIDROXILASE (DEFICIÊNCIA); GENES (CLASSIFICAÇÃO); MUTAÇÃO GENÉTICA; FENÓTIPOS; HIPERTENSÃO
- Language: Inglês
- Imprenta:
- Publisher place: Springfield
- Date published: 2009
- Source:
- Título: Journal of clinical endocrinology and metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 94, n. 9, p. 3481-3485, 2009
-
ABNT
SOARDI, Fernanda C. et al. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism, v. 94, n. 9, p. 3481-3485, 2009Tradução . . Acesso em: 28 dez. 2025. -
APA
Soardi, F. C., Penachioni, J. Y., Justo, G. Z., Bachega, T. A. S. S., Inácio, M., Mendonça, B. B. de, et al. (2009). Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism, 94( 9), 3481-3485. -
NLM
Soardi FC, Penachioni JY, Justo GZ, Bachega TASS, Inácio M, Mendonça BB de, Castro M de, Mello MP de. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism. 2009 ; 94( 9): 3481-3485.[citado 2025 dez. 28 ] -
Vancouver
Soardi FC, Penachioni JY, Justo GZ, Bachega TASS, Inácio M, Mendonça BB de, Castro M de, Mello MP de. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism. 2009 ; 94( 9): 3481-3485.[citado 2025 dez. 28 ] - Análise da região promotora do gene HESX1 em pacientes com deficiência hormonal hipofisária combinada (DHHC) sem mutações na região codoficadora do HESX1
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