The Golgi complex lies at the heart of the secretory pathway and is responsible for modifying proteins and lipids, as well as sorting newly synthesized molecules to their correct destination. As a consequence of these important roles, any changes in its proteome can negatively affect its function and in turn lead to disease. Recently, a number of proteins have been identified, which when either depleted or mutated, result in diseases that affect various organ systems. Here we describe how these proteins have been linked to the Golgi complex, and specifically how they affect either the morphology, membrane traffic or glycosylation ability of this organelle. © 2013 by the authors; licensee MDPI, Basel, Switzerland.
CITATION STYLE
Bexiga, M. G., & Simpson, J. C. (2013, September 10). Human diseases associated with form and function of the Golgi complex. International Journal of Molecular Sciences. https://doi.org/10.3390/ijms140918670
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