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Feast or famine: Role of TRPML in preventing cellular amino acid starvation
Lysosomal storage diseases are metabolic disorders characterized by the accumulation of acidic vacuoles, and are usually the consequence of the deficiency of an enzyme responsible for the metabolism of vesicular lipids, proteins or carbohydrates. In contrast, mucolipidosis type IV (MLIV), results fr...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Landes Bioscience
2013
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3542223/ https://ncbi.nlm.nih.gov/pubmed/23047439 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/auto.22260 |
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