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Immune modulation in Pompe disease treated with enzyme replacement therapy

2012; Taylor & Francis; Volume: 8; Issue: 6 Linguagem: Inglês

10.1586/eci.12.40

1744-8409

Suhrad G. Banugaria, Trusha Patel, Priya S. Kishnani,

Carbohydrate Chemistry and Synthesis

Pompe disease is a lysosomal storage disease characterized by massive glycogen deposition in skeletal, cardiac and smooth muscle secondary to the deficiency of acid α-glucosidase (GAA) [1]. Once ra...