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Glycogen Storage Disease Type III
An autosomal recessive inherited type of glycogen storage disease caused by deficiency of the glycogen debranching enzyme. It results in the accumulation of structurally abnormal glycogen in the heart, skeletal muscles, and/or liver. (NCI Thesaurus)
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A stainable aggregation of glycogen in the cytoplasm.
An extracellular coating of polymeric sugars or glycoproteins.
