Seizures Are Regulated by Ubiquitin-specific Peptidase 9 X-linked (USP9X), a De-Ubiquitinase

Epilepsy is a common disabling disease with complex, multifactorial genetic and environmental etiology. The small fraction of epilepsies subject to Mendelian inheritance offers key insight into epilepsy disease mechanisms; and pathologies brought on by mutations in a single gene can point the way to...

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書誌詳細
出版年:PLoS Genet
主要な著者: Paemka, Lily, Mahajan, Vinit B., Ehaideb, Salleh N., Skeie, Jessica M., Tan, Men Chee, Wu, Shu, Cox, Allison J., Sowers, Levi P., Gecz, Jozef, Jolly, Lachlan, Ferguson, Polly J., Darbro, Benjamin, Schneider, Amy, Scheffer, Ingrid E., Carvill, Gemma L., Mefford, Heather C., El-Shanti, Hatem, Wood, Stephen A., Manak, J. Robert, Bassuk, Alexander G.
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2015
主題:
Research Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4357451/
https://ncbi.nlm.nih.gov/pubmed/25763846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1005022
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