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Published in 2022 at "Neuropediatrics"
DOI: 10.1055/a-2060-4576
Abstract: Abstract Autosomal dominant mutations of the KCNQ2 gene can cause two epileptic disorders: benign familial neonatal seizures (BFNS) and developmental epileptic encephalopathy (DEE). This systematic review aims to identify the best reported therapy for these…
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Keywords:
phenotype;
antiseizure medication;
genotype;
systematic review ... See more keywords