https://www.selleckchem.com/pr....oducts/AZD2281(Olapa
he CUP classifier to the clinical picture and pathology investigations before performing additional investigations.Glycogen storage disease type 0 (GSD is an autosomal recessive disorder caused by a sequence variant in the GYS2 gene, leading to decreased or absent activity of hepatic glycogen synthase. With a frequency of less than 1 in 1,000,000 individuals, GSD0 represents only around 1% of all glycogen storage disease cases but it might be underrecognized. A 13-month-old girl of reportedly unrelated parents presented with
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