1. Chen, Y. T. in The Metabolic and Molecular Bases of Inherited Disease, 8th edn. (eds. Scriver, C.R., Beaudet, A.L., Sly, W.S. & Valle, D.) 1521–1551 (McGraw-Hill, New York, 2001).
2. Shin, Y. S. Glycogen storage disease: clinical, biochemical, and molecular heterogeneity. Semin. Pediatr. Neurol. 13, 115–120 (2006).
3. Hers, H. G., Verhue, W. & Mathieu, M. in Control of Glycogen Metabolism (eds. Whelan, W.J. & Cameron, M.P.) 151–175 (J. & A. Churchill, London, 1964).
4. Van Hoof, F. & Hers, H. G. The subgroups of type 3 glycogenosis. Eur. J. Biochem. 2, 265–270 (1967).
5. Howell, R. R. & Williams, J. C. in The Metabolic Basis of Inherited Disease, 5th edn. (eds. Stanbury, J.B., Wyngaarden, J.B., Fredrickson, D.S., Goldstein, J.L. & Brown, M.S.) 141–166 (McGraw-Hill, New York, 1983).