Association between KCNQ2, TCF4 and RGS18 polymorphisms and silent brain infarction based on whole­exome sequencing.

Kim, Jung Oh; Lee, Kee Ook; Kim, Hyun Woo; Park, Han Sung; Kim, Jinkwon; Sung, Jung Hoon; Oh, Doyeun; Kim, Ok Joon; Kim, Nam Keun

Association between KCNQ2, TCF4 and RGS18 polymorphisms and silent brain infarction based on wholeexome sequencing.

Kim, Jung Oh; Lee, Kee Ook; Kim, Hyun Woo; Park, Han Sung; Kim, Jinkwon; Sung, Jung Hoon; Oh, Doyeun; Kim, Ok Joon; Kim, Nam Keun.

Afiliação

Kim JO; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, Gyeonggi 13488, Republic of Korea.
Lee KO; Department of Neurology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam, Gyeonggi 13496, Republic of Korea.
Kim HW; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, Gyeonggi 13488, Republic of Korea.
Park HS; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, Gyeonggi 13488, Republic of Korea.
Kim J; Department of Neurology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam, Gyeonggi 13496, Republic of Korea.
Sung JH; Department of Cardiology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam, Gyeonggi 13496, Republic of Korea.
Oh D; Department of Internal Medicine, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam, Gyeonggi 13496, Republic of Korea.
Kim OJ; Department of Neurology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam, Gyeonggi 13496, Republic of Korea.
Kim NK; Department of Biomedical Science, College of Life Science, CHA University, Seongnam, Gyeonggi 13488, Republic of Korea.

Mol Med Rep ; 21(4): 1973-1983, 2020 04.

Article em En | MEDLINE | ID: mdl-32319632

Assuntos

Infarto Encefálico/genética; Sequenciamento do Exoma; Estudos de Associação Genética; Predisposição Genética para Doença; Canal de Potássio KCNQ2/genética; Polimorfismo de Nucleotídeo Único/genética; Proteínas RGS/genética; Fator de Transcrição 4/genética; Alelos; Estudos de Casos e Controles; Feminino; Frequência do Gene/genética; Humanos; Masculino; Pessoa de Meia-Idade

Palavras-chave

silent brain infarction; prevalence; risk factors; casecontrol studies; single nucleotide polymorphism

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Infarto Encefálico / Proteínas RGS / Polimorfismo de Nucleotídeo Único / Canal de Potássio KCNQ2 / Estudos de Associação Genética / Fator de Transcrição 4 / Sequenciamento do Exoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Mol Med Rep Ano de publicação: 2020 Tipo de documento: Article

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