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Loss of CLN7 results in depletion of soluble lysosomal proteins and impaired mTOR reactivation
Defects in the MFSD8 gene encoding the lysosomal membrane protein CLN7 lead to CLN7 disease, a neurodegenerative lysosomal storage disorder belonging to the group of neuronal ceroid lipofuscinoses. Here, we have performed a SILAC-based quantitative analysis of the lysosomal proteome using Cln7-defic...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5932567/ https://ncbi.nlm.nih.gov/pubmed/29514215 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy076 |
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