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BACKGROUND Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome; MPS VI) is an autosomal recessive lysosomal storage disorder in which deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B; ARSB) leads to the storage of glycosaminoglycans (GAGs) in connective tissue. The genotype-phenotype correlation has been addressed in several publications(More)
The lack of available deceased donors and the immunological incompatibility between the patients and their voluntary donor candidates make kidney exchange among donor-patient pairs a preferable solution performed locally by many organ transplantation centers in Turkey. However, maximum benefit from kidney exchange can only be achieved when the donor patient(More)
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