Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://www.nature.com/articles/nrendo.2010.189.pdf
Reference122 articles.
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3. Lei, K.-J., Shelly, L. L., Pan, C.-J., Sidbury, J. B. & Chou, J. Y. Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a. Science 262, 580–583 (1993).
4. Lei, K.-J., Pan, C.-J., Shelly, L. L., Liu, J.-L. & Chou, J. Y. Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a. J. Clin. Invest. 93, 1994–1999 (1994).
5. Hiraiwa, H., Pan, C.-J., Lin, B., Moses, S. W. & Chou, J. Y. Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b. J. Biol. Chem. 274, 5532–5536 (1999).
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