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: Blackwell Publishing

Document Type: Research article

DOI: 10.1111/j.1528-1167.2008.01549_2.x

Links for this article

http://www.ingentaconnect.com/bsc/epi/2008/00000049/00000006/art00023
http://openurl.ingenta.com/content?genre=article&issn=0013-9580&volume=49&issue=6&spage=1104&epage=1107
http://dx.doi.org/10.1111/j.1528-1167.2008.01549_2.x