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Preview | Issue Date | Title | Author(s) |
---|---|---|---|
2010 | De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin | Heron, S.; Scheffer, I.; Iona, X.; Zuberi, S.; Birch, R.; McMahon, J.; Bruce, C.; Berkovic, S.; Mulley, J. |
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- 1 2010