Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder (2016)
- Authors:
- USP affiliated authors: PEREIRA, CARLOS ALBERTO DE BRAGANCA - IME ; MIGUEL FILHO, EURIPEDES CONSTANTINO - FM ; BRENTANI, HELENA PAULA - FM
- Unidades: IME; FM
- DOI: 10.1186/s12868-016-0313-4
- Assunto: BIOESTATÍSTICA
- Keywords: OCD; Methylation; Oxytocin receptor gene (OXTR)
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: BMC Neuroscience
- ISSN: 1471-2202
- Volume/Número/Paginação/Ano: v. 17, n. 1, [8 p.], 2016
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by-nc-nd
-
ABNT
CAPPI, Carolina et al. Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder. BMC Neuroscience, v. 17, n. 1, p. [8 ], 2016Tradução . . Disponível em: https://doi.org/10.1186/s12868-016-0313-4. Acesso em: 28 dez. 2025. -
APA
Cappi, C., Diniz, J. B., Requena, G. de L., Lourenço, T., Lisboa, B. C. G., Batistuzzo, M. C., et al. (2016). Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder. BMC Neuroscience, 17( 1), [8 ]. doi:10.1186/s12868-016-0313-4 -
NLM
Cappi C, Diniz JB, Requena G de L, Lourenço T, Lisboa BCG, Batistuzzo MC, Marques AH, Hoexter MQ, Pereira CA de B, Miguel EC, Brentani H. Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder [Internet]. BMC Neuroscience. 2016 ; 17( 1): [8 ].[citado 2025 dez. 28 ] Available from: https://doi.org/10.1186/s12868-016-0313-4 -
Vancouver
Cappi C, Diniz JB, Requena G de L, Lourenço T, Lisboa BCG, Batistuzzo MC, Marques AH, Hoexter MQ, Pereira CA de B, Miguel EC, Brentani H. Epigenetic evidence for involvement of the oxytocin receptor gene in obsessive–compulsive disorder [Internet]. BMC Neuroscience. 2016 ; 17( 1): [8 ].[citado 2025 dez. 28 ] Available from: https://doi.org/10.1186/s12868-016-0313-4 - Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways
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Informações sobre o DOI: 10.1186/s12868-016-0313-4 (Fonte: oaDOI API)
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