Assessment of genetic variant burden in epilepsy-associated brain lesions

It is challenging to estimate genetic variant burden across different subtypes of epilepsy. Herein, we used a comparative approach to assess the genetic variant burden and genotype–phenotype correlations in four most common brain lesions in patients with drug-resistant focal epilepsy. Targeted seque...

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Publicado en:Eur J Hum Genet
Autores principales: Niestroj, Lisa-Marie, May, Patrick, Artomov, Mykyta, Kobow, Katja, Coras, Roland, Pérez-Palma, Eduardo, Altmüller, Janine, Thiele, Holger, Nürnberg, Peter, Leu, Costin, Palotie, Aarno, Daly, Mark J., Klein, Karl Martin, Beschorner, Rudi, Weber, Yvonne G., Blümcke, Ingmar, Lal, Dennis
Formato: Artigo
Lenguaje:Inglês
Publicado: Springer International Publishing 2019
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6871528/
https://ncbi.nlm.nih.gov/pubmed/31358956
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-019-0484-4
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