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: 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: 12 jan. 2026. -
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 2026 jan. 12 ] 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 2026 jan. 12 ] Available from: https://doi.org/10.20945/2359-3997000000139 - Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly
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Informações sobre o DOI: 10.20945/2359-3997000000139 (Fonte: oaDOI API)
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