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Published in 2019 at "Frontiers in Neurology"
DOI: 10.3389/fneur.2019.00064
Abstract: Mutations in the Potassium channel subfamily T member 1 (KCNT1) gene have been reported in a range of epileptic encephalopathies. Here we report the case of a 12-year-old male suffering from multiple types of epileptic…
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Keywords:
kcnt1 mutation;
lennox gastaut;
syndrome kcnt1;
gastaut syndrome ... See more keywords