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Biochemical and clinical studies on 4 cases of hepatic glycogen storage disease

โœ Scribed by Sano, Masaju


Publisher
Springer-Verlag
Year
1971
Tongue
English
Weight
663 KB
Volume
6
Category
Article
ISSN
0435-1339

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Glycogen storage disease type 1a in Isra
โœ Parvari, Ruti; Lei, Ke-Jian; Bashan, Nava; Hershkovitz, Eli; Korman, Stanley H.; ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 33 KB ๐Ÿ‘ 2 views

Glycogen storage disease type 1a (von Gierke disease, GSD 1a) is caused by the deficiency of microsomal glucose-6-phosphatase (G6Pase) activity which catalyzes the final common step of glycogenolysis and gluconeogenesis. The recent cloning of the G6Pase cDNA and characterization of the human G6Pase