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Autor:
Xiaodan Ding, Don S. Anson, Chantelle McIntyre, Ainslie L.K. Derrick-Roberts, Carmen E. Macsai, Sharon Byers, Krystyna H. Zarrinkalam, Paul H. Anderson
Publikováno v:
Molecular Genetics and Metabolism. 106:202-213
Mucopolysaccharidosis VII (MPS VII) is an autosomal recessive, lysosomal storage disorder caused by β-glucuronidase (GUSB) deficiency, resulting in the accumulation of glycosaminoglycans (GAGs), in a variety of cell types. Severe, progressive skelet