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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.

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Bibliographic Details
Title: Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.
Authors: Epi4K consortium (CORPORATE AUTHOR), Epilepsy Phenome/Genome Project (CORPORATE AUTHOR)
Source: Lancet Neurology. Feb2017, Vol. 16 Issue 2, p135-143. 9p.
Database: Academic Search Ultimate
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An: 120709108
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PubType: Academic Journal
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  Data: Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.
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  Data: <searchLink fieldCode="AR" term="%22Epi4K+consortium%22">Epi4K consortium</searchLink> (CORPORATE AUTHOR)<br /><searchLink fieldCode="AR" term="%22Epilepsy+Phenome%2FGenome+Project%22">Epilepsy Phenome/Genome Project</searchLink> (CORPORATE AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Lancet+Neurology%22">Lancet Neurology</searchLink>. Feb2017, Vol. 16 Issue 2, p135-143. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=120709108
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      – Type: doi
        Value: 10.1016/S1474-4422(16)30359-3
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      – Code: eng
        Text: English
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        StartPage: 135
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      – TitleFull: Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.
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              Text: Feb2017
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              Y: 2017
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