Solving the unsolved genetic epilepsies: Current and future perspectives.

Johannesen, Katrine M; Tümer, Zeynep; Weckhuysen, Sarah; Barakat, Tahsin Stefan; Bayat, Allan

Johannesen, Katrine M; Tümer, Zeynep; Weckhuysen, Sarah; Barakat, Tahsin Stefan; Bayat, Allan.

Afiliação

Johannesen KM; Department of Genetics, Copenhagen University Hospital, Copenhagen, Denmark.
Tümer Z; Department of Epilepsy Genetics and Personalized Medicine, The Danish Epilepsy Center, Dianalund, Denmark.
Weckhuysen S; Department of Genetics, Copenhagen University Hospital, Copenhagen, Denmark.
Barakat TS; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Bayat A; Applied and Translational Neurogenomics Group, VIB Centre for Molecular Neurology, Antwerp, Belgium.

Epilepsia ; 64(12): 3143-3154, 2023 Dec.

Article em En | MEDLINE | ID: mdl-37750451

Assuntos

Epilepsia; Variação Genética; Humanos; Variação Genética/genética; Epilepsia/diagnóstico; Epilepsia/genética; Exoma; Sequenciamento do Exoma; Mapeamento Cromossômico

Palavras-chave

DNA methylation; epilepsy; epilepsy genetics; metabolomics; non-coding regions; re-analysis; somatic mosaicism; transcriptomics

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Epilepsia Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo

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PubMed Links

Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Epilepsia Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article