KCNQ2 -Related Epilepsy: Genotype–Phenotype Relationship with Tailored Antiseizure Medication (ASM)—A Systematic Review
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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… read more here.
Keywords: phenotype; antiseizure medication; genotype; systematic review ... See more keywords