Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type la
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb02674.x/fullpdf
Reference22 articles.
1. Cornstarch therapy in type 1 glycogen storage disease;Chen;N Engl J Med,1984
2. Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type la;Lei;Science,1993
3. Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17;Brody;Genomics,1995
4. 22 genes from chromosome 17q21: cloning, sequencing, and characterization of mutations in breast cancer families and tumors;Friedman;Genomics,1995
5. Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type la mouse;Lei;Nat Genet,1996
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