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A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years.
Epilepsia. 2006 May;47(5):851-9. doi: 10.1111/j.1528-1167.2006.00552.x.
Epilepsia. 2006.
PMID: 16686649
Free article.
Gene symbol: KCNQ2. Disease: Benign neonatal familial convulsion.
Pinto D, de Haan GJ, Carton D, Bader A, Witte J, Peters E, van Erp MG, Vandereyken W, Boezeman EH, Boon P, Halley DJ, Koeleman BP, Lindhout D.
Pinto D, et al. Among authors: vandereyken w.
Hum Genet. 2005 Jul;117(2-3):300.
Hum Genet. 2005.
PMID: 16156031
No abstract available.
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