Glycogen storage disease type III (GSD III; McKusick, 232,400) is an autosomal recessive disease caused by the deficiency of glycogen-debranching enzyme (amylo-1,6-glucosidase, AGL). AGL contains two ...
Mycobacterial species deploy intricate pathways to synthesise and remodel glycogen-like α-glucans and complex polysaccharides that underpin both energy storage and pathogenicity. Intracellular ...
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