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

Thomas, Rhys 2017. Ultra-rare genetic variation in common epilepsies: a case-control sequencing study. The Lancet Neurology 16 (2) , pp. 135-143. 10.1016/S1474-4422(16)30359-3

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Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Subjects: R Medicine > R Medicine (General)
Publisher: Elsevier
ISSN: 1474-4422
Date of First Compliant Deposit: 16 February 2017
Date of Acceptance: 23 November 2016
Last Modified: 05 Jun 2017 19:27
URI: http://orca.cf.ac.uk/id/eprint/98346

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