Bodamer O.De Jesus V.Keutzer J.Zhang K.WUH-LIANG HWUM?hl A.2020-12-162020-12-1620080149-2918https://www.scopus.com/inward/record.uri?eid=2-s2.0-40749129999&doi=10.1016%2fS0149-2918%2808%2980022-7&partnerID=40&md5=5192ee8d00633b9d9a35d3545179ab9dhttps://scholars.lib.ntu.edu.tw/handle/123456789/525980[SDGs]SDG3glucan 1,4 alpha glucosidase; article; blood examination; cardiomyopathy; diagnostic accuracy; early diagnosis; enzyme activity; enzyme assay; enzyme replacement; Fabry disease; feasibility study; fluorometry; Gaucher disease; globoid cell leukodystrophy; glycogen storage disease type 2; human; lysosome storage disease; muscle hypotonia; newborn screening; sensitivity and specificity; tandem mass spectrometryjournal article10.1016/S0149-2918(08)80022-72-s2.0-40749129999