DOI:
10.1055/s-00000041
Neuropediatrics
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References
Soldovieri MV, Boutry-Kryza N, Milh M. , et al.
Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A.
Hum Mutat 2014;
35 (03) 356-367
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