Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome (2008)
- Authors:
- Autor USP: CASTRO, MARGARET DE - FMRP
- Unidade: FMRP
- Subjects: SÍNDROME DE KALLMANN; ENDOCRINOLOGIA; METABOLISMO
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2008
- Source:
- Título: Journal of Clinical Endocrinology and Metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 93, n. 10, p. 4113-4118, 2008
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ABNT
ABREU, Ana Paula et al. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism, v. 93, n. 10, p. 4113-4118, 2008Tradução . . Acesso em: 12 mar. 2026. -
APA
Abreu, A. P., Trarbach, E. B., Castro, M. de, Costa, E. M. F., Versiani, B., Baptista, M. T. M., et al. (2008). Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism, 93( 10), 4113-4118. -
NLM
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 10): 4113-4118.[citado 2026 mar. 12 ] -
Vancouver
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Baptista MTM, Garmes HM, Mendonça BB, Latronico AC. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. Journal of Clinical Endocrinology and Metabolism. 2008 ; 93( 10): 4113-4118.[citado 2026 mar. 12 ] - TAC3/TACR3 mutations reveal preferential activation of GnRH release by neurokinin B in neonatal life followed by reversal in adulthood
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