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HARVARD Citation
Heron, S. et al. (2010). De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin. Journal of medical genetics. 47 (2), pp. 137-141. [Online].
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Heron, S. et al. (2010). De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin. Journal of medical genetics. 47 (2), pp. 137-141. [Online].