Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier

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Bibliographic Details
Published in:Seizure (London, England) England), 2019-03, Vol.66, p.1-3
Main Authors: Nass, Robert Daniel, Hansen, Niels, Quesada, Carlos, Rüber, Theodor, Kornblum, Cornelia, Zsurka, Gábor, Hermann, Philipp, Becker, Albert, Gärtner, Florian, Hattingen, Elke, Block, Wolfgang, Steidl, Eike, Elger, Christian E., Surges, Rainer, Kunz, Wolfram S.
Format: Article
Language:English
Subjects:
Adult
Epilepsies, Partial - diagnosis
Epilepsies, Partial - genetics
GTP Phosphohydrolases - genetics
Heterozygote
Humans
Male
Mitochondrial Diseases - diagnosis
Mitochondrial Diseases - genetics
Mitochondrial retinoencephalopathy
Occipital lobe epilepsy
OPA-1
Retinal Diseases - diagnosis
Retinal Diseases - genetics
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ISSN:1059-1311
1532-2688
DOI:10.1016/j.seizure.2019.01.029