Leber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic
Author:
Publisher
Informa UK Limited
Subject
Ophthalmology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/08820538.2015.1115251
Reference97 articles.
1. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
2. The Clinical Characteristics of Pedigrees of Leber's Hereditary Optic Neuropathy With the 11778 Mutation
3. Sequence and organization of the human mitochondrial genome
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1. GenEye24: Novel rapid screening test for the top-3 Leber’s Hereditary Optic Neuropathy pathogenic sequence variants;Mitochondrion;2023-03
2. Terapia genética de injeção intravítrea de rAAV2-ND4 para neuropatia óptica hereditária de Leber: uma revisão sistemática;Revista Brasileira de Oftalmologia;2023
3. Gene therapy restores mitochondrial function and protects retinal ganglion cells in optic neuropathy induced by a mito-targeted mutant ND1 gene;Gene Therapy;2022-04-06
4. Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber’s hereditary optic neuropathy;Irish Journal of Medical Science (1971 -);2021-05-29
5. Mitochondrial 13513G>A Mutation With Low Mutant Load Presenting as Isolated Leber's Hereditary Optic Neuropathy Assessed by Next Generation Sequencing;Frontiers in Neurology;2021-03-04
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