Identification of cerebral spinal fluid protein biomarkers in Niemann-Pick disease, type C1

Abstract Background Niemann-Pick disease, type C1 (NPC1) is an ultrarare, recessive, lethal, lysosomal disease characterized by progressive cerebellar ataxia and cognitive impairment. Although the NPC1 phenotype is heterogeneous with variable age of onset, classical NPC1 is a pediatric disorder. Cur...

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Main Authors: Kiersten Campbell, Niamh X. Cawley, Rachel Luke, Katelin E. J. Scott, Nicholas Johnson, Nicole Y. Farhat, Derek Alexander, Christopher A. Wassif, Wenping Li, Stephanie M. Cologna, Elizabeth Berry-Kravis, An Dang Do, Ryan K. Dale, Forbes D. Porter
Format: Article
Language:English
Published: BMC 2023-01-01
Series:Biomarker Research
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Online Access:https://doi.org/10.1186/s40364-023-00448-x

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