1. Pembridge, Olivia G, Wallace, Natalie S, Clements, Thomas P, Jackson, Lauren P. 2022. AP-4 loss in CRISPR-edited zebrafish affects early embryo development. In Advances in biological regulation, 87, 100945. doi:10.1016/j.jbior.2022.100945. https://pubmed.ncbi.nlm.nih.gov/36642642/
2. Mattera, Rafael, De Pace, Raffaella, Bonifacino, Juan S. . The role of AP-4 in cargo export from the trans-Golgi network and hereditary spastic paraplegia. In Biochemical Society transactions, 48, 1877-1888. doi:10.1042/BST20190664. https://pubmed.ncbi.nlm.nih.gov/33084855/
3. Hardies, Katia, May, Patrick, Djémié, Tania, De Jonghe, Peter, Hirst, Jennifer. 2014. Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly. In Human molecular genetics, 24, 2218-27. doi:10.1093/hmg/ddu740. https://pubmed.ncbi.nlm.nih.gov/25552650/
4. Mattera, Rafael, Park, Sang Yoon, De Pace, Raffaella, Guardia, Carlos M, Bonifacino, Juan S. 2017. AP-4 mediates export of ATG9A from the trans-Golgi network to promote autophagosome formation. In Proceedings of the National Academy of Sciences of the United States of America, 114, E10697-E10706. doi:10.1073/pnas.1717327114. https://pubmed.ncbi.nlm.nih.gov/29180427/
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