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

Epi4K consortium, Epilepsy Phenome/Genome Project and Bellows, Susannah T. 2017, Ultra-rare genetic variation in common epilepsies: a case-control sequencing study, Lancet neurology, vol. 16, no. 2, pp. 135-143, doi: 10.1016/S1474-4422(16)30359-3.

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Title Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
Author(s) Epi4K consortium
Epilepsy Phenome/Genome Project
Bellows, Susannah T.
Journal name Lancet neurology
Volume number 16
Issue number 2
Start page 135
End page 143
Total pages 9
Publisher Elsevier
Place of publication Amsterdam, The Netherlands
Publication date 2017-02
ISSN 1474-4422
1474-4465
Keyword(s) Case-Control Studies
Epilepsies, Partial
Epilepsy, Generalized
Exome
Genetic Predisposition to Disease
Genetic Variation
Humans
Sequence Analysis, DNA
Epi4K consortium
Epilepsy Phenome/Genome Project
Science & Technology
Life Sciences & Biomedicine
Clinical Neurology
Neurosciences & Neurology
ONSET EPILEPTIC ENCEPHALOPATHY
GENOME
DISEASE
QUINIDINE
SEIZURES
MUTATION
RISK
Language eng
DOI 10.1016/S1474-4422(16)30359-3
Field of Research 1103 Clinical Sciences
1109 Neurosciences
HERDC Research category C1 Refereed article in a scholarly journal
ERA Research output type C Journal article
Copyright notice ©2016, Elsevier
Persistent URL http://hdl.handle.net/10536/DRO/DU:30109462

Document type: Journal Article
Collection: School of Psychology
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