Author:
Zhang X. Kate,Elbin Carole S.,Turecek Frantisek,Scott Ronald,Chuang Wei-Lien,Keutzer Joan M.,Gelb Michael
Reference11 articles.
1. Scriver C. R., Beaudet A. L., Sly W. S., Valle D. eds. (2001) The Metabolic and Molecular Bases of Inherited Disease, 8th ed. New York, NY: McGraw-Hill.
2. Meikle P. J., Hopwood J. J. (2003) Lysosomal storage disorders: emerging therapeutic options require early diagnosis. Eur J Pediatr, 162: S34–S7.
3. Clarke L. A. (2008) The mucopolysaccharidoses: a success of molecular medicine. Expert Rev Mol Med
10(1): e1.
4. Rohrbach M, Clarke J. T. (2007) Treatment of lysosomal storage disorders: progress with enzyme replacement therapy. Drugs
67: 2697–716.
5. Chien Y.-H., Chiang S.-C., Zhang X. K., Keutzer J. M., Lee N.-C., Huang A.-C., Chen C.-A., Wu M.-H., Huang P.-H., Tsai F.-J., Chen Y.-T., Hwu W.-L. (2008) Early detection of Pompe disease by newborn screening is feasible: results from the Taiwan screening program. Pediatrics
122: e39–e45.
Cited by
25 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献