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

Thomas, Rhys ORCID: https://orcid.org/0000-0003-2062-8623 2017. Ultra-rare genetic variation in common epilepsies: a case-control sequencing study. 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)
Additional Information:	Epi4K consortium, Epilepsy Phenome/Genome Project
Publisher:	Elsevier: Lancet
ISSN:	1474-4422
Date of First Compliant Deposit:	16 February 2017
Date of Acceptance:	23 November 2016
Last Modified:	19 Nov 2024 00:30
URI:	https://orca.cardiff.ac.uk/id/eprint/98346

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