Heterozygous loss of function of <i>NR4A2</i> is associated with intellectual deficiency, rolandic epilepsy, and language impairment.

Ramos, Luiza L P; Monteiro, Fabiola P; Sampaio, Leticia P B; Costa, Larissa A; Ribeiro, Mara D O; Freitas, Erika L; Kitajima, Joao P; Kok, Fernando

Heterozygous loss of function of NR4A2 is associated with intellectual deficiency, rolandic epilepsy, and language impairment.

Ramos, Luiza L P; Monteiro, Fabiola P; Sampaio, Leticia P B; Costa, Larissa A; Ribeiro, Mara D O; Freitas, Erika L; Kitajima, Joao P; Kok, Fernando.

Afiliação

Ramos LLP; Mendelics Genomic Analysis Sao Paulo Brazil.
Monteiro FP; Mendelics Genomic Analysis Sao Paulo Brazil.
Sampaio LPB; Department of Neurology University of Sao Paulo School of Medicine Sao Paulo Brazil.
Costa LA; Mendelics Genomic Analysis Sao Paulo Brazil.
Ribeiro MDO; Mendelics Genomic Analysis Sao Paulo Brazil.
Freitas EL; Mendelics Genomic Analysis Sao Paulo Brazil.
Kitajima JP; Mendelics Genomic Analysis Sao Paulo Brazil.
Kok F; Mendelics Genomic Analysis Sao Paulo Brazil.

Clin Case Rep ; 7(8): 1582-1584, 2019 Aug.

Article em En | MEDLINE | ID: mdl-31428396

Palavras-chave

NR4A2; intellectual deficiency; rolandic epilepsy

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article