https://www.selleckchem.com/pr....oducts/picropodophyl
Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.Objective To describe clinical, biochemical, and molecular genetic findings in a large inbred family in which 4 children with a severe early-onset epileptic-dyskinetic encephalopathy, with suppression burst EEG, harbored homozygous mutations of phosphatidylinositol glycan anchor biosynthesis, class P (PIGP), a member of the large glycosylphosphatidylinositol (GPI) anchor biosynthesis gene family. Methods We studied clinical features, EEG
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