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Abnormal gene expression in cerebellum of Npc1-/- mice during postnatal development
Niemann-Pick Type C disease is an autosomal recessive neurodegenerative disorder with abnormal lipid storage as the major cellular pathologic hallmark. Genetic analyses have identified mutations in NPC1 gene in the great majority of cases, while mutations in NPC2 account for the remainders. Yet, lit...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2848886/ https://ncbi.nlm.nih.gov/pubmed/20153740 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2010.02.019 |
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