Cite
MLA Citation
Stefania Magri et al.. “Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation.” Human mutation, vol. 39, no. 12, 2018, pp. 2060–2071. http://access.bl.uk/ark:/81055/vdc_100073412239.0x00004a