Leber Hereditary Optic Neuropathy Caused by a Mitochondrial DNA 10663T>C Point Mutation and Its Response to Idebenone Treatment
| Autor: | Øystein Kalsnes Jørstad, Eva Meling Ødegaard, Ketil Riddervold Heimdal, Emilia Kerty |
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| Rok vydání: | 2018 |
| Předmět: |
Mitochondrial DNA
LEBER HEREDITARY OPTIC NEUROPATHY Consensus Ubiquinone business.industry Point mutation Optic Atrophy Hereditary Leber DNA Mitochondrial 03 medical and health sciences Ophthalmology chemistry.chemical_compound 0302 clinical medicine chemistry 030221 ophthalmology & optometry medicine Cancer research Humans Point Mutation Idebenone Neurology (clinical) business 030217 neurology & neurosurgery DNA medicine.drug |
| Zdroj: | Journal of Neuro-Ophthalmology. 38:129-131 |
| ISSN: | 1070-8022 |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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