Fonte: Clinical case reports. Unidade: FM
Assuntos: PESSOAS COM DEFICIÊNCIA INTELECTUAL, EPILEPSIA, TRANSTORNOS DA LINGUAGEM, PROTEÍNAS NUCLEARES, MUTAÇÃO GENÉTICA, DELEÇÃO DE GENES
ABNT
RAMOS, Luiza L. P et al. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment. Clinical case reports, v. 7, n. 8, p. 1582-1584, 2019Tradução . . Disponível em: https://doi.org/10.1002/ccr3.2260. Acesso em: 18 ago. 2024.APA
Ramos, L. L. P., Monteiro, F. P., Sampaio, L. P. B., Costa, L. A., Ribeiro, M. D. O., Freitas, E. L., et al. (2019). Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment. Clinical case reports, 7( 8), 1582-1584. doi:10.1002/ccr3.2260NLM
Ramos LLP, Monteiro FP, Sampaio LPB, Costa LA, Ribeiro MDO, Freitas EL, Kitajima JP, Kok F. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment [Internet]. Clinical case reports. 2019 ; 7( 8): 1582-1584.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1002/ccr3.2260Vancouver
Ramos LLP, Monteiro FP, Sampaio LPB, Costa LA, Ribeiro MDO, Freitas EL, Kitajima JP, Kok F. Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment [Internet]. Clinical case reports. 2019 ; 7( 8): 1582-1584.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1002/ccr3.2260