Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type la

WUH-LIANG HWUChuang S.-C.Tsai L.-P.MEI-HWEI CHANGChuang S.-M.Wang T.-R.2020-12-162020-12-1619950964-6906https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029042475&doi=10.1093%2fhmg%2f4.6.1095&partnerID=40&md5=e284220e3eb98aad4b742cfa54ed91c1https://scholars.lib.ntu.edu.tw/handle/123456789/526107[SDGs]SDG3glucose 6 phosphatase; article; child; chinese; clinical article; exon; female; gene; gene mutation; glycogen storage disease type 1; human; male; priority journal; single strand conformation polymorphism; Child; Child, Preschool; Female; Follow-Up Studies; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Human; Infant; Male; Mongoloid Race; Mutation; Support, Non-U.S. Gov'tGlucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type lajournal article10.1093/hmg/4.6.109576554662-s2.0-0029042475