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Quoted phrase not found in phrase index: "Seizures, benign familial neonatal, 2"
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A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan.
Lee IC, Yang JJ, Li SY. Lee IC, et al. J Formos Med Assoc. 2017 Sep;116(9):711-719. doi: 10.1016/j.jfma.2016.11.009. Epub 2016 Dec 27. J Formos Med Assoc. 2017. PMID: 28038823 Free article.
METHODS: We studied the KCNQ2 genotype from 75 nonconsanguineous patients with childhood epilepsy without an identified cause (age range: from 2 days to 18 years) and from 55 healthy adult controls without epilepsy. ...We also analyzed 10 affected family members with the s …
METHODS: We studied the KCNQ2 genotype from 75 nonconsanguineous patients with childhood epilepsy without an identified cause (age range: fr …