CMT2A Harboring Mitofusin 2 Mutation with Optic Nerve Atrophy and Normal Visual Acuity

CMT2A Harboring Mitofusin 2 Mutation with Optic Nerve Atrophy and Normal Visual Acuity

Silvana Guerriero,1 Francesco D’Oria,1 Giacomo Rossetti,2 Rosa Anna Favale,1 Stefano Zoccolella,1 Giovanni Alessio,1 Vittoria Petruzzella1 1Department of Medical Science, Neuroscience and Sense Organs, University of Bari Aldo Moro, Bari, Italy; 2Department of Molecular Biology, University...

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Bibliographic Details
Main Authors: Guerriero S, D'Oria F, Rossetti G, Favale RA, Zoccolella S, Alessio G, Petruzzella V
Format: Article
Language:English
Published: Dove Medical Press 2020-02-01
Series:International Medical Case Reports Journal
Subjects:
charcot-marie-tooth type 2a
mitofusin2
optic atrophy
mitochondria
visual field.
Online Access:https://www.dovepress.com/cmt2a-harboring-mitofusin-2-mutation-with-optic-nerve-atrophy-and-norm-peer-reviewed-article-IMCRJ

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https://www.dovepress.com/cmt2a-harboring-mitofusin-2-mutation-with-optic-nerve-atrophy-and-norm-peer-reviewed-article-IMCRJ

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