Fonte: Current Genetic Medicine Reports. Unidade: IB
Assuntos: NEUROGENÉTICA, PESSOAS COM DEFICIÊNCIA INTELECTUAL, VARIAÇÃO GENÉTICA
ABNT
MACHADO, Ana Claudia Dantas et al. ACTB loss-of-function variant and AUTS2 duplication in a patient with syndromic intellectual disability. Current Genetic Medicine Reports, v. 13, 2025Tradução . . Disponível em: https://doi.org/10.1007/s40142-025-00213-6. Acesso em: 27 nov. 2025.APA
Machado, A. C. D., Carvalho, L. M. L., Vasconcelos, F. T. G. R. de, Bertola, D. R., Rosenberg, C., & Krepischi, A. C. V. (2025). ACTB loss-of-function variant and AUTS2 duplication in a patient with syndromic intellectual disability. Current Genetic Medicine Reports, 13. doi:10.1007/s40142-025-00213-6NLM
Machado ACD, Carvalho LML, Vasconcelos FTGR de, Bertola DR, Rosenberg C, Krepischi ACV. ACTB loss-of-function variant and AUTS2 duplication in a patient with syndromic intellectual disability [Internet]. Current Genetic Medicine Reports. 2025 ; 13[citado 2025 nov. 27 ] Available from: https://doi.org/10.1007/s40142-025-00213-6Vancouver
Machado ACD, Carvalho LML, Vasconcelos FTGR de, Bertola DR, Rosenberg C, Krepischi ACV. ACTB loss-of-function variant and AUTS2 duplication in a patient with syndromic intellectual disability [Internet]. Current Genetic Medicine Reports. 2025 ; 13[citado 2025 nov. 27 ] Available from: https://doi.org/10.1007/s40142-025-00213-6
