Infantile-onset Pompe disease is an inherited disorder that is normally diagnosed within the first months of life. It is caused by lack of or defect in an enzyme (a special protein that carries out normal chemical reactions within the body) called acid alpha-glucosidase (GAA). GAA normally breaks...
Here, we have determined rhGAA ADA epitopes in the plasma samples of Pompe disease patients using series of affinity purifications combined with epitope extraction and label free quantitation LC-MS methodology
