Autumn[removed]Volume 19 No 2 CONTENTS Chairman’s Chat

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Date: 2013-06-25 13:27:20 Lipid storage disorders Neurodegenerative disorders Niemann–Pick disease NPC1 Niemann-Pick disease type C Lysosomal storage disease Tay–Sachs disease National Institutes of Health Genetic Alliance UK Health Rare diseases Medicine		Autumn[removed]Volume 19 No 2 CONTENTS Chairman’s Chat Add to Reading List Source URL: www.nnpdf.org Download Document from Source Website File Size: 2,67 MB Share Document on Facebook

	Exercise – Exploring sequence variant annotation in human The NPC1 (Niemann-Pick disease, type C1) gene encodes a protein that is thought to be involved in the intracellular transport of cholesterol. One of the varian DocID: 1u8ku - View Document
	FOR EMBARGOED USE ONLY Vtesse, Inc. Initiates Phase 2b/3 Clinical Trial of VTS-270 for Treatment of Niemann-Pick Type C1 (NPC) Disease • • DocID: 1lXBa - View Document
	3rd Annual BALTIMORE ORIOLES DILLON PAPIER’S BIRTHDAY BENEFIT Proceeds will fund Type C research for THE NATIONAL NIEMANN-PICK DISEASE FOUNDATION Enjoy a ball game with friends and family on DocID: 1kTMM - View Document
	WORKSHOP SUMMARY Sponsored by: Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA) Office of the Commissioner, Office of Orphan Products Development (OOPD), FDA National Institutes of Healt DocID: ZxYc - View Document
	Product Datasheet Anti-Acid sphingomyelinase antibody [mAbcam74281] ab74281 1 Abreviews DocID: QysL - View Document