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Wiley, Human Mutation: Variation, Informatics and Disease, 12(39), p. 2060-2071, 2018
DOI: 10.1002/humu.23658
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Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation
Journal article published in 2018 by
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
,
Chiara Pantaleoni,
Franco Taroni
This paper is made freely available by the publisher.
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