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Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy
Although there are many known Mendelian genes linked to epileptic or developmental and epileptic encephalopathy (EE/DEE), its genetic architecture is not fully explained. Here, we address this incompleteness by analyzing exomes of 743 EE/DEE cases and 2366 controls. We observe that damaging ultra-ra...
Tallennettuna:
Julkaisussa: | Nat Commun |
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Päätekijät: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
Nature Publishing Group UK
2019
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6555845/ https://ncbi.nlm.nih.gov/pubmed/31175295 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-10482-9 |
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