Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery (2019)
- Authors:
- USP affiliated authors: JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.20945/2359-3997000000139
- Subjects: HORMÔNIOS DA ADENO-HIPÓFISE; MUTAÇÃO GENÉTICA; GENES HOMEOBOX
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Rio De Janeiro, Rj
- Date published: 2019
- Source:
- Título do periódico: Archives of endocrinology metabolism
- ISSN: 2359-3997
- Volume/Número/Paginação/Ano: v. 63, n. 2, p. 167-174, 2019
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
CORREA, Fernanda A et al. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery. Archives of endocrinology metabolism, v. 63, n. 2, p. 167-174, 2019Tradução . . Disponível em: https://doi.org/10.20945/2359-3997000000139. Acesso em: 01 maio 2024. -
APA
Correa, F. A., Nakaguma, M., Madeira, J. L. O., Nishi, M. Y., Abrao, M. G., Jorge, A. A. de L., et al. (2019). Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery. Archives of endocrinology metabolism, 63( 2), 167-174. doi:10.20945/2359-3997000000139 -
NLM
Correa FA, Nakaguma M, Madeira JLO, Nishi MY, Abrao MG, Jorge AA de L, Carvalho LR, Arnhold IJP, Mendonça BB de. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery [Internet]. Archives of endocrinology metabolism. 2019 ; 63( 2): 167-174.[citado 2024 maio 01 ] Available from: https://doi.org/10.20945/2359-3997000000139 -
Vancouver
Correa FA, Nakaguma M, Madeira JLO, Nishi MY, Abrao MG, Jorge AA de L, Carvalho LR, Arnhold IJP, Mendonça BB de. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery [Internet]. Archives of endocrinology metabolism. 2019 ; 63( 2): 167-174.[citado 2024 maio 01 ] Available from: https://doi.org/10.20945/2359-3997000000139 - Investigação genética
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- Molecular analysis of brazilian patients with combined pituitary hormone deficiency (CPHD) and orthotopic posterior pituitary lobe (OPP) reveals 8 different PROP1 alterations with three novel mutations
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Informações sobre o DOI: 10.20945/2359-3997000000139 (Fonte: oaDOI API)
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