Concurrent AFG3L2 and...

Human Mutation 2018 / 09

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

Magri, Stefania, Fracasso, Valentina, Plumari, Massimo, Alfei, Enrico, Ghezzi, Daniele, Gellera, Cinzia, Rusmini, Paola, Poletti, Angelo, Bella, Daniela Di, Elia, Antonio E., Pantaleoni, Chiara, Taron
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Language:
english
Journal:
Human Mutation
DOI:
10.1002/humu.23658
Date:
September, 2018
File:
PDF, 2.15 MB
english, 2018
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