Understanding rare variant contributions to autism: lessons from dystrophin-deficient model (2025)
Source: npj Genomic Medicine. Unidades: IB, Interunidades em Bioinformática, IP, FM
Subjects: GENÉTICA MÉDICA, TRANSTORNO AUTÍSTICO, DISTROFIA MUSCULAR, VARIAÇÃO GENÉTICA
ABNT
COSTA, Claudia Ismania Samogi et al. Understanding rare variant contributions to autism: lessons from dystrophin-deficient model. npj Genomic Medicine, v. 10, n. 18, 2025Tradução . . Disponível em: https://doi.org/10.1038/s41525-025-00469-5. Acesso em: 08 out. 2025.APA
Costa, C. I. S., Madanelo, L., Wang, J. Y. T., Campos, G. da S., Girardi, A. C. D. S., Scliar, M., et al. (2025). Understanding rare variant contributions to autism: lessons from dystrophin-deficient model. npj Genomic Medicine, 10( 18). doi:10.1038/s41525-025-00469-5NLM
Costa CIS, Madanelo L, Wang JYT, Campos G da S, Girardi ACDS, Scliar M, Monfardini F, Pavanello R de CM, Cória VR, Vibranovski M, Krepischi ACV, Lourenço NCV, Zatz M, Yamamoto GL, Zachi EC, Passos-Bueno MR. Understanding rare variant contributions to autism: lessons from dystrophin-deficient model [Internet]. npj Genomic Medicine. 2025 ; 10( 18):[citado 2025 out. 08 ] Available from: https://doi.org/10.1038/s41525-025-00469-5Vancouver
Costa CIS, Madanelo L, Wang JYT, Campos G da S, Girardi ACDS, Scliar M, Monfardini F, Pavanello R de CM, Cória VR, Vibranovski M, Krepischi ACV, Lourenço NCV, Zatz M, Yamamoto GL, Zachi EC, Passos-Bueno MR. Understanding rare variant contributions to autism: lessons from dystrophin-deficient model [Internet]. npj Genomic Medicine. 2025 ; 10( 18):[citado 2025 out. 08 ] Available from: https://doi.org/10.1038/s41525-025-00469-5