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7. Di Bella, Daniela, Lazzaro, Federico, Brusco, Alfredo, Muzi-Falconi, Marco, Taroni, Franco. 2010. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. In Nature genetics, 42, 313-21. doi:10.1038/ng.544. https://pubmed.ncbi.nlm.nih.gov/20208537/
8. Caporali, Leonardo, Magri, Stefania, Legati, Andrea, Carelli, Valerio, Taroni, Franco. 2020. ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy. In Annals of neurology, 88, 18-32. doi:10.1002/ana.25723. https://pubmed.ncbi.nlm.nih.gov/32219868/
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