A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings (2010)
- Authors:
- Autor USP: JORGE, ALEXANDER AUGUSTO DE LIMA - FM
- Unidade: FM
- DOI: 10.1530/EJE-10-0272
- Subjects: ENDOCRINOPATIAS (PATOLOGIA;FISIOPATOLOGIA); MUTAÇÃO GENÉTICA; DOENÇAS PULMONARES INTERSTICIAIS; SISTEMA IMUNE (FISIOPATOLOGIA); PROLACTINA (FISIOPATOLOGIA)
- Language: Inglês
- Imprenta:
- Source:
- Título: European Journal of Endocrinology
- ISSN: 0804-4643
- Volume/Número/Paginação/Ano: v. 163, n. 2, p. 349-355, 2010
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
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ABNT
PIRES, Patricia N. Pugliese et al. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, v. 163, n. 2, p. 349-355, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0272. Acesso em: 28 fev. 2026. -
APA
Pires, P. N. P., Tonelli, C. A., Dora, J. M., Silva, P. C. A., Czepielewski, M., Simoni, G., et al. (2010). A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, 163( 2), 349-355. doi:10.1530/EJE-10-0272 -
NLM
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2026 fev. 28 ] Available from: https://doi.org/10.1530/EJE-10-0272 -
Vancouver
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2026 fev. 28 ] Available from: https://doi.org/10.1530/EJE-10-0272 - The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?
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Informações sobre o DOI: 10.1530/EJE-10-0272 (Fonte: oaDOI API)
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