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![]() Date: 2015-11-17 16:51:10Biology Cell biology Anatomy Cellular processes Vesicles NPC1 Cardiology Lipoproteins Cholesterol Lysosomal storage disease LAMP1 Low-density lipoprotein | Add to Reading List |
![]() | How one patient with a rare disease coped with his genetic disorderDocID: 1r9mW - View Document |
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![]() | What is HUNTER SYNDROME? Hunter syndrome, or mucopolysaccharidosis II (MPS II), is a rare and progressive lysosomal storage disease inherited in an X-linked recessiveDocID: 1lIxr - View Document |
![]() | MUCOPOLYSACCHARIDOSES Rare Diseases Unit of the Finnish Association of People with Physical Disabilities Support for this guide was provided by Genzyme.DocID: 1fJSQ - View Document |
![]() | May 27, 2014 BioMarin Doses First Patient in Phase 3 INSPIRE Trial With BMN 701 for the Treatment of Pompe Disease Proprietary Glycosylation Independent Lysosomal Targeting (GILT) Tagging Technology Has Been Shown to ImDocID: 1aiEg - View Document |