Early HSCT corrects the skeleton in MPS.
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2015-03
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In this issue of Blood, Pievani et al have identified a potential solution to the remaining barrier to the success of hematopoietic stem cell transplantation (HSCT) in children with severe phenotype Hurler syndrome (mucopolysaccharidosis type I [MPS I]).
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Kurtzberg, Joanne (2015). Early HSCT corrects the skeleton in MPS. Blood, 125(10). pp. 1518–1519. 10.1182/blood-2014-11-606681 Retrieved from https://hdl.handle.net/10161/24633.
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