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A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
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
Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case.
Fister P, Soltirovska-Salamon A, Debeljak M, Paro-Panjan D.
Fister P, et al.
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
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