Deeksha Bali is Director of the Duke Glycogen Storage Disease laboratory and has been highly involved in laboratory diagnosis and research on Pompe disease and other glycogen storage diseases for the past 15 years. New methods for non-invasive diagnosis of lysosomal storage diseases have been developed so that patients can benefit from early diagnosis and initiation of treatment.
Predicting cross-reactive immunological material (CRIM) status in Pompe disease using GAA mutations: Lessons learned from 10 years of clinical laboratory testing experience†
Article first published 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 40–49, 15 February 2012
How to Cite
Bali, D. S., Goldstein, J. L., Banugaria, S., Dai, J., Mackey, J., Rehder, C. and Kishnani, P. S. (2012), Predicting cross-reactive immunological material (CRIM) status in Pompe disease using GAA mutations: Lessons learned from 10 years of clinical laboratory testing experience. Am. J. Med. Genet., 160C: 40–49. doi: 10.1002/ajmg.c.31319
How to cite this article: Bali DS, Goldstein JL, Banugaria S, Dai J, Mackey J, Rehder C, Kishnani PS. 2012. Predicting cross-reactive immunological material (CRIM) status in Pompe disease using GAA mutations: Lessons learned from 10 years of clinical laboratory testing experience. Am J Med Genet Part C Semin Med Genet 160C:40–49.
- Issue published online: 23 JAN 2012
- Article first published online: 17 JAN 2012
- Genzyme Corporation and by the Lysosomal Disease Network (LDN)
- National Center for Research Resources (NCRR). Grant Number: UL1RR024128
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