A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD) (2016)
- Authors:
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; MONTENEGRO, LUCIANA RIBEIRO - FM ; MACHADO, UBIRATAN FABRES - ICB ; MENDONÇA, BERENICE BILHARINHO DE - FM ; FREITAS, HELAYNE SOARES DE - ICB
- Unidades: FM; ICB
- DOI: 10.1530/eje-15-0149
- Subjects: GRAVIDEZ DE GÊMEOS; HORMÔNIO DO CRESCIMENTO; EXPRESSÃO GÊNICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: European journal of endocrinology
- ISSN: 0804-4643
- Volume/Número/Paginação/Ano: v. 175, n. 02, p. K7-K15, 2016
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
MADEIRA, João L. O. et al. A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD). European journal of endocrinology, v. 175, n. 02, p. K7-K15, 2016Tradução . . Disponível em: https://doi.org/10.1530/eje-15-0149. Acesso em: 18 abr. 2024. -
APA
Madeira, J. L. O., Jorge, A. A. de L., Martin, R. M., Montenegro, L. R., Franca, M. M., Costalong, E. F., et al. (2016). A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD). European journal of endocrinology, 175( 02), K7-K15. doi:10.1530/eje-15-0149 -
NLM
Madeira JLO, Jorge AA de L, Martin RM, Montenegro LR, Franca MM, Costalong EF, Correa FA, Otto AP, Arnhold IJP, Freitas HS, Machado UF, Mendonça BB de, Carvalho LR. A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD) [Internet]. European journal of endocrinology. 2016 ; 175( 02): K7-K15.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1530/eje-15-0149 -
Vancouver
Madeira JLO, Jorge AA de L, Martin RM, Montenegro LR, Franca MM, Costalong EF, Correa FA, Otto AP, Arnhold IJP, Freitas HS, Machado UF, Mendonça BB de, Carvalho LR. A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD) [Internet]. European journal of endocrinology. 2016 ; 175( 02): K7-K15.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1530/eje-15-0149 - A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reducd GH1 expression in siblings with isolated GH deficiency (IGHD)
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Informações sobre o DOI: 10.1530/eje-15-0149 (Fonte: oaDOI API)
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