A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency (2005)
- Autores:
- Autor USP: MENDONCA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assuntos: HIPERTENSÃO (ETIOLOGIA); MUTAÇÃO GENÉTICA; BRASILEIROS; HORMÔNIOS SEXUAIS (ANORMALIDADES)
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Program and Abstracts
- Nome do evento: The Endocrine Society's Annual Meeting
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ABNT
MARTIN, Regina M. et al. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 19 abr. 2024. -
APA
Martin, R. M., Costa, E. F., Arnhold, I. J. P., & Mendonça, B. B. (2005). A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Martin RM, Costa EF, Arnhold IJP, Mendonça BB. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. Program and Abstracts. 2005 ;[citado 2024 abr. 19 ] -
Vancouver
Martin RM, Costa EF, Arnhold IJP, Mendonça BB. A homozigous 25 Bp duplication (Nt 4157-4181) at exon 5 in the CYP17 resulting in a premature stop codon as a new cause of combined 17alpha-hydroxylase/17,20-lyase deficiency. Program and Abstracts. 2005 ;[citado 2024 abr. 19 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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