Defective platelet function in Niemann‐Pick disease type C1

Niemann‐Pick disease type C (NPC) is a neurodegenerative lysosomal storage disorder caused by mutations in either NPC1 (95% of cases) or NPC2. Reduced late endosome/lysosome calcium (Ca(2+)) levels and the accumulation of unesterified cholesterol and sphingolipids within the late endocytic system ch...

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Bibliografiske detaljer
Udgivet i:JIMD Rep
Main Authors: Chen, Oscar C. W., Colaco, Alexandria, Davis, Lianne C., Kiskin, Fedir N., Farhat, Nicole Y., Speak, Anneliese O., Smith, David A., Morris, Lauren, Eden, Emily, Tynan, Patricia, Churchill, Grant C., Galione, Antony, Porter, Forbes D., Platt, Frances M.
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley & Sons, Inc. 2020
Fag:
Research Reports
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7653256/
https://ncbi.nlm.nih.gov/pubmed/33204596
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12148
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