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Publication Detail
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study
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Publication Type:Journal article
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Publication Sub Type:Article
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Authors:Koko M, Motelow JE, Stanley KE, Bobbili DR, Dhindsa RS, May P
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Publisher:WILEY
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Publication date:15/01/2022
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Pagination:723, 735
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Journal:EPILEPSIA
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Volume:63
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Issue:3
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Status:Published
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Print ISSN:0013-9580
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Language:English
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Keywords:Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, familial epilepsy, GABA(A) receptors, GABRG2, GGE, sporadic epilepsy, CHILDHOOD ABSENCE EPILEPSY, COMMON EPILEPSIES, MUTATION, GAMMA-2-SUBUNIT, GENOME
Abstract
No abstract found
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