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Multiplex newborn screening for Pompe, Fabry, Hunter, Gaucher, and Hurler diseases using a digital microfluidic platform:

A recently published study in the International Journal for Clinical Chemistry describes how new therapies for lysosomal storage disorders (LSDs) have generated interest in screening newborns for these conditions.  You may find more information on the published study by following this link: http://www.ncbi.nlm.nih.gov/pubmed/23660237