Cite

    Magri, S., Fracasso, V., Plumari, M., Alfei, E., Ghezzi, D., Gellera, C., Rusmini, P., Poletti, A., Di Bella, D., Elia, A. E., Pantaleoni, C., & Taroni, F. (2018). concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation. Human mutation, 39(12), 2060–2071. http://access.bl.uk/ark:/81055/vdc_100073412239.0x00004a