1. Vantaggiato, Chiara, Clementi, Emilio, Bassi, Maria Teresa. 2013. ZFYVE26/SPASTIZIN: a close link between complicated hereditary spastic paraparesis and autophagy. In Autophagy, 10, 374-5. doi:10.4161/auto.27173. https://pubmed.ncbi.nlm.nih.gov/24284334/
2. Özdemir, Taha Reşid, Gençpınar, Pınar, Arıcan, Pınar, Dündar, Nihal Olgaç, Özyılmaz, Berk. 2019. A case of spastic paraplegia-15 with a novel pathogenic variant in ZFYVE26 gene. In The International journal of neuroscience, 129, 1198-1202. doi:10.1080/00207454.2019.1653293. https://pubmed.ncbi.nlm.nih.gov/31385551/
3. Algahtani, Hussein, Shirah, Bader, Aljohani, Rahaf, Abdulkareem, Angham Abdulrhman, Naseer, Muhammad Imran. . Adult-Onset Hereditary Spastic Paraplegia 15 in a Saudi Patient with A Compound Heterozygous Variant in the ZFYVE26Gene. In Maedica, 17, 730-734. doi:10.26574/maedica.2022.17.3.730. https://pubmed.ncbi.nlm.nih.gov/36540605/
4. Vinci, Mirella, Fchera, Marco, Antonino Musumeci, Sebastiano, Cali, Francesco, Aurelio Vitello, Girolamo. . Novel c.C2254T (p.Q752*) mutation in ZFYVE26 (SPG15) gene in a patient with hereditary spastic paraparesis. In Journal of genetics, 97, 1469-1472. doi:. https://pubmed.ncbi.nlm.nih.gov/30555096/
5. Lai, Ze-Hua, Liu, Xiao-Ying, Song, Yuan-Yue, Zhou, Hai-Yan, Zeng, Li-Li. 2023. Case report: Hereditary spastic paraplegia with a novel homozygous mutation in ZFYVE26. In Frontiers in neurology, 14, 1160110. doi:10.3389/fneur.2023.1160110. https://pubmed.ncbi.nlm.nih.gov/37681008/
6. Khundadze, Mukhran, Kollmann, Katrin, Koch, Nicole, Beetz, Christian, Hübner, Christian A. 2013. A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system. In PLoS genetics, 9, e1003988. doi:10.1371/journal.pgen.1003988. https://pubmed.ncbi.nlm.nih.gov/24367272/
7. Garg, Vranda, André, Selina, Heyer, Luisa, Dosch, Roland, Geurten, Bart R H. 2024. Axon demyelination and degeneration in a zebrafish spastizin model of hereditary spastic paraplegia. In Open biology, 14, 240100. doi:10.1098/rsob.240100. https://pubmed.ncbi.nlm.nih.gov/39503232/
8. Bibi, Farah, Efthymiou, Stephanie, Bourinaris, Thomas, Saeed, Sadia, Minhas, Nasir Mahmood. 2020. Rare novel CYP2U1 and ZFYVE26 variants identified in two Pakistani families with spastic paraplegia. In Journal of the neurological sciences, 411, 116669. doi:10.1016/j.jns.2020.116669. https://pubmed.ncbi.nlm.nih.gov/32006740/