Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathy
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference28 articles.
1. URF6, Last Unidentified Reading Frame of Human mtDNA, Codes for an NADH Dehydrogenase Subunit
2. Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase
3. Mitochondrial Inheritance in a Mitochondrially Mediated Disease
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1. Mitochondrially Targeted Gene Therapy Rescues Visual Loss in a Mouse Model of Leber’s Hereditary Optic Neuropathy;International Journal of Molecular Sciences;2023-12-02
2. Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington’s disease;Ultrastructural Pathology;2022-08-10
3. Prognostic factors for visual acuity in patients with Leber's hereditary optic neuropathy after rAAV2‐ND4 gene therapy;Clinical & Experimental Ophthalmology;2019-05-08
4. Nouvelle mutation de l’ADN mitochondrial dans la neuropathie optique héréditaire de Leber : à propos d’un cas;Journal Français d'Ophtalmologie;2018-06
5. Visual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation;BMC Ophthalmology;2017-10-18
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