Defective platelet function in Niemann‐Pick disease type C1
Abstract 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 (Ca2+) levels and the accumulation of unesterified cholesterol and sphingolipids within the late endocytic sy...
Główni autorzy: | , , , , , , , , , , , , , |
---|---|
Format: | Artykuł |
Język: | English |
Wydane: |
Wiley
2020-11-01
|
Seria: | JIMD Reports |
Hasła przedmiotowe: | |
Dostęp online: | https://doi.org/10.1002/jmd2.12148 |