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Quoted phrase not found in phrase index: "Seizures, benign familial neonatal, 2"
Page 1
A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan.
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 …
A novel de novo KCNQ2 mutation in a child with treatmentresistant early-onset epileptic encephalopathy.
Benetou C, Papailiou S, Maritsi D, Anagnostopoulou K, Kontos H, Vartzelis G.
Benetou C, et al.
Turk J Pediatr. 2019;61(2):279-281. doi: 10.24953/turkjped.2019.02.020.
Turk J Pediatr. 2019.
PMID: 31951342
Free article.
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