The attenuated/late onset lysosomal storage disorders: Therapeutic goals and indications for enzyme replacement treatment in Gaucher and Fabry disease

doi:10.1016/j.beem.2014.08.006

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The attenuated/late onset lysosomal storage disorders: Therapeutic goals and indications for enzyme replacement treatment in Gaucher and Fabry disease

26 Aug 2014

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PMID: 25987174
DOI: 10.1016/j.beem.2014.08.006

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