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

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. Currently t...

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Detalles Bibliográficos
Autores principales: Campbell, Kiersten, Cawley, Niamh X., Luke, Rachel, Scott, Katelin E. J., Johnson, Nicholas, Farhat, Nicole Y., Alexander, Derek, Wassif, Christopher A., Li, Wenping, Cologna, Stephanie M., Berry-Kravis, Elizabeth, Do, An Dang, Dale, Ryan K., Porter, Forbes D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887810/
https://www.ncbi.nlm.nih.gov/pubmed/36721240
http://dx.doi.org/10.1186/s40364-023-00448-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887810/
https://www.ncbi.nlm.nih.gov/pubmed/36721240
http://dx.doi.org/10.1186/s40364-023-00448-x

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