CLN3 is required for the clearance of glycerophosphodiesters from lysosomes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
https://www.nature.com/articles/s41586-022-05221-y.pdf
Reference52 articles.
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2. Medoh, U. N., Chen, J. Y. & Abu-Remaileh, M. Lessons from metabolic perturbations in lysosomal storage disorders for neurodegeneration. Curr. Opin. Syst. Biol. 29, 100408 (2022).
3. Platt, F. M., d'Azzo, A., Davidson, B. L., Neufeld, E. F. & Tifft, C. J. Lysosomal storage diseases. Nat. Rev. Dis. Primers 4, 27 (2018).
4. Ferguson, S. M. Neuronal lysosomes. Neurosci. Lett. 697, 1–9 (2019).
5. Perera, R. M. & Zoncu, R. The lysosome as a regulatory hub. Annu. Rev. Cell Dev. Biol. 32, 223–253 (2016).
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