Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy

Source: Epilepsia, Volume 49, Number 6, June 2008 , pp. 1104-1107(4)

Publisher: Wiley-Blackwell

Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1528-1167.2008.01549_2.x

Publication date: 2008-06-01

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• In this Subject: Neurology & Psychiatry

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