SCIENTIFIC LITERATURE · MED

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

Magri S, Fracasso V, Plumari M, Alfei E, Ghezzi D, Gellera C, Rusmini P, Poletti A, Di Bella D, Elia AE, Pantaleoni C, Taroni F.

Hum Mutat · 2018-10-10

DOI: 10.1002/humu.23658PMID: 30252181

Check source for accessResearch Support, Non-U.S. Gov't; Journal Article; Case ReportsOriginal source ↗

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