Source:http://linkedlifedata.com/resource/umls/id/C0002272
MSH: Enzymes that catalyze the exohydrolysis of 1,4-alpha-glucosidic linkages with release of alpha-glucose. Deficiency of alpha-1,4-glucosidase may cause GLYCOGEN STORAGE DISEASE TYPE II.,CSP: hydrolyses terminal, non-reducing 1,4-linked alpha-D- glucose residues with release of alpha-D-glucose.