Gene network analysis identifies dysregulated pathways in an autism spectrum disorder caused by mutations in Transcription Factor 4 (2025)
- Authors:
- Autor USP: CAMARGO, ANTÔNIO PEDRO DE CASTELLO BRANCO DA ROCHA - IQ
- Unidade: IQ
- DOI: 10.1002/cbdv.202402311
- Subjects: TRANSTORNO AUTÍSTICO; GENES
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Scientific Reports
- ISSN: 2045-2322
- Volume/Número/Paginação/Ano: v. 15, p. 1-15 art. 4993, 2025
- Status:
- Artigo possui acesso gratuito no site do editor (Bronze Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
CARVALHO, Lucas M. de et al. Gene network analysis identifies dysregulated pathways in an autism spectrum disorder caused by mutations in Transcription Factor 4. Scientific Reports, v. 15, p. 1-15 art. 4993, 2025Tradução . . Disponível em: https://dx.doi.org/10.1002/cbdv.202402311. Acesso em: 08 abr. 2026. -
APA
Carvalho, L. M. de, Vinicius M. A. Carvalho,, Camargo, A. P., & Papes, F. (2025). Gene network analysis identifies dysregulated pathways in an autism spectrum disorder caused by mutations in Transcription Factor 4. Scientific Reports, 15, 1-15 art. 4993. doi:10.1002/cbdv.202402311 -
NLM
Carvalho LM de, Vinicius M. A. Carvalho, Camargo AP, Papes F. Gene network analysis identifies dysregulated pathways in an autism spectrum disorder caused by mutations in Transcription Factor 4 [Internet]. Scientific Reports. 2025 ; 15 1-15 art. 4993.[citado 2026 abr. 08 ] Available from: https://dx.doi.org/10.1002/cbdv.202402311 -
Vancouver
Carvalho LM de, Vinicius M. A. Carvalho, Camargo AP, Papes F. Gene network analysis identifies dysregulated pathways in an autism spectrum disorder caused by mutations in Transcription Factor 4 [Internet]. Scientific Reports. 2025 ; 15 1-15 art. 4993.[citado 2026 abr. 08 ] Available from: https://dx.doi.org/10.1002/cbdv.202402311 - Abnormal expression of splicing regulators RBFOX and NOVA is associated with aberrant splicing patterns at the Neurexin-3 gene in a monogenic autism spectrum disorder
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