Multiplex Newborn Screening for Pompe, Fabry, Hunter, Gaucher, and Hurler Diseases Using a Digital Microfluidic Platform

This report describes the feasibility of performing a multiplex assay using digital microfluidic technology to screen for lysosomal storage disorders.

Authors: Ramakrishna S. Sista, Tong Wang, Ning Wu, Carrie Graham, Allen Eckhardt, Theodore Winger, Vijay Srinivasan, Deeksha Bali, David S. Millington, and Vamsee K. Pamula

Clin Chim Acta. 2013 September 23; 424: 12–18. doi:10.1016/j.cca.2013.05.001.