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Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case.
Eur J Paediatr Neurol. 2013 May;17(3):308-10. doi: 10.1016/j.ejpn.2012.10.007. Epub 2012 Nov 10.
Eur J Paediatr Neurol. 2013.
PMID: 23146207
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B.
Li H, et al.
Epilepsy Res. 2008 Mar;79(1):1-5. doi: 10.1016/j.eplepsyres.2007.12.005. Epub 2008 Feb 4.
Epilepsy Res. 2008.
PMID: 18249525
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