Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier.
Nass, Robert Daniel
Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier. [electronic resource] - Seizure Mar 2019 - 1-3 p. digital
Publication Type: Case Reports; Letter
1532-2688
10.1016/j.seizure.2019.01.029 doi
Adult
Epilepsies, Partial--diagnosis
GTP Phosphohydrolases--genetics
Heterozygote
Humans
Male
Mitochondrial Diseases--diagnosis
Retinal Diseases--diagnosis
Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier. [electronic resource] - Seizure Mar 2019 - 1-3 p. digital
Publication Type: Case Reports; Letter
1532-2688
10.1016/j.seizure.2019.01.029 doi
Adult
Epilepsies, Partial--diagnosis
GTP Phosphohydrolases--genetics
Heterozygote
Humans
Male
Mitochondrial Diseases--diagnosis
Retinal Diseases--diagnosis