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A novel mutation in the glucose-6-phosphatase gene in Korean twins with glycogen storage disease type Ia.

作者信息

Goto M, Taki T, Sugie H, Miki Y, Kato H, Hayashi Y

机构信息

Department of Pediatrics, Faculty of Medicine, University of Tokyo, Japan.

出版信息

J Inherit Metab Dis. 2000 Dec;23(8):851-2. doi: 10.1023/a:1026777106212.

DOI:10.1023/a:1026777106212
PMID:11196115
Abstract
摘要

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本文引用的文献

1
Asparagine-linked oligosaccharides are localized to a luminal hydrophilic loop in human glucose-6-phosphatase.
J Biol Chem. 1998 Aug 21;273(34):21658-62. doi: 10.1074/jbc.273.34.21658.
2
Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a.导致1a型糖原贮积病的葡萄糖-6-磷酸酶基因突变。
Science. 1993 Oct 22;262(5133):580-3. doi: 10.1126/science.8211187.