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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Official URL: http://dx.doi.org/10.1016/S1474-4422(16)30359-3
| Item Type: | Article |
|---|---|
| Date Type: | Publication |
| Status: | Published |
| Schools: | Schools > Medicine Research Institutes & Centres > 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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