Source: Journal of clinical endocrinology and metabolism. Unidades: FM, FMRP
Subjects: HIDROXILASE (DEFICIÊNCIA), GENES (CLASSIFICAÇÃO), MUTAÇÃO GENÉTICA, FENÓTIPOS, HIPERTENSÃO
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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: 01 nov. 2024.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 2024 nov. 01 ]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 2024 nov. 01 ]
