Defects in the retina of Niemann-pick type C 1 mutant mice

BACKGROUND: Niemann-Pick type C1 (NPC1) disease is an inherited lysosomal storage disease caused by mutation of the Npc1 gene, resulting in a progressive accumulation of unesterified cholesterol and glycolipids in lysosomes of multiple tissues and leading to neurodegeneration and other disease. In N...

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Detalles Bibliográficos
Autores principales: Yan, Xin, Ma, Lucy, Hovakimyan, Marina, Lukas, Jan, Wree, Andreas, Frank, Marcus, Guthoff, Rudolf, Rolfs, Arndt, Witt, Martin, Luo, Jiankai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267119/
https://www.ncbi.nlm.nih.gov/pubmed/25472750
http://dx.doi.org/10.1186/s12868-014-0126-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267119/
https://www.ncbi.nlm.nih.gov/pubmed/25472750
http://dx.doi.org/10.1186/s12868-014-0126-2

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