Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment (2019)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1002/ccr3.2260
- Subjects: PESSOAS COM DEFICIÊNCIA INTELECTUAL; EPILEPSIA; TRANSTORNOS DA LINGUAGEM; PROTEÍNAS NUCLEARES; MUTAÇÃO GENÉTICA; DELEÇÃO DE GENES
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical case reports
- ISSN: 2050-0904
- Volume/Número/Paginação/Ano: v. 7, n. 8, p. 1582-1584, 2019
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
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: 04 mar. 2026. -
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/ccr3.2260 -
NLM
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 2026 mar. 04 ] Available from: https://doi.org/10.1002/ccr3.2260 -
Vancouver
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 2026 mar. 04 ] Available from: https://doi.org/10.1002/ccr3.2260 - Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP
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Informações sobre o DOI: 10.1002/ccr3.2260 (Fonte: oaDOI API)
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