In this Special Issue dedicated to the pioneer of cystinosis research Dr. Jerry Schneider, the state-of-the-art understanding of cellular and molecular mechanisms of various disease features is highlighted, opening new horizons for innovative treatment strategies for cystinosis and potentially other lysosomal storage diseases.
This special issue is endorsed by the European Rare Kidney Disease Reference Network (ERKNet).
https://doi.org/10.3390/books978-3-0365-4567-7
