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Targeted resequencing in epileptic encephalopathies ident... | ResearchHub
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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
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Authors
Gemma Carvill
33 more
Gemma Carvill
•
Sinéad Heavin
31 more
•
Heather Mefford
Published
May 26, 2013
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Journal
Nature Genetics
Topics
Biology
Neuroscience
Medicine
Internal Medicine
Genetics
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DOI
10.1038/ng.2646
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature Genetics
Topics
Biology
Neuroscience
Medicine
Internal Medicine
Genetics
Show all topics
DOI
10.1038/ng.2646
Other Formats
PDF