Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation

Human Mutation,Volume 0, Issue ja, -Not available-.

Source: Human Mutation - September 25, 2018 Category: Genetics & Stem Cells Authors: Stefania Magri, Valentina Fracasso, Massimo Plumari, Enrico Alfei, Daniele Ghezzi, Cinzia Gellera, Paola Rusmini, Angelo Poletti, Daniela Di Bella, Antonio E. Elia, Chiara Pantaleoni, Franco Taroni Source Type: research