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Enhanced expression of manganese-dependent superoxide dismutase in human and sheep CLN6 tissues.
Neuronal ceroid lipofuscinosis type 6 and its sheep model (OCL6) are lysosomal storage disorders caused by mutations in the CLN6 gene product of unknown function. It has been proposed that mitochondrial dysfunction, including defects in mitochondrial protein degradation, organelle enlargement and fu...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1223781/ https://ncbi.nlm.nih.gov/pubmed/12946273 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20030598 |
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