Sarah P. Young (Pediatrics Medical Genetics, Duke University Medical Center, North Carolina) is the assistant director of the Duke Biochemical Genetics Laboratory. The main focus of her research is the development and application of biomarker assays for inherited metabolic diseases, including Pompe disease and other lysosomal storage disorders.
Assessing disease severity in Pompe disease: The roles of a urinary glucose tetrasaccharide biomarker and imaging techniques†
Version of Record online: 17 JAN 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Special Issue: Advancements in Pompe Disease
Volume 160C, Issue 1, pages 50–58, 15 February 2012
How to Cite
Young, S. P., Piraud, M., Goldstein, J. L., Zhang, H., Rehder, C., Laforet, P., Kishnani, P. S., Millington, D. S., Bashir, M. R. and Bali, D. S. (2012), Assessing disease severity in Pompe disease: The roles of a urinary glucose tetrasaccharide biomarker and imaging techniques. Am. J. Med. Genet., 160C: 50–58. doi: 10.1002/ajmg.c.31320
How to cite this article: Young SP, Piraud M, Goldstein JL, Zhang H, Rehder C, Laforet P, Kishnani PS, Millington DS, Bashir M, Bali D. 2012. Assessing disease severity in Pompe disease: The roles of a urinary glucose tetrasaccharide biomarker and imaging techniques. Am J Med Genet Part C Semin Med Genet 160C:50–58.
- Issue online: 23 JAN 2012
- Version of Record online: 17 JAN 2012
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