Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy-Reference-Cited by-同舟云学术

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Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy

Published:2002-10-24 Issue:5 Volume:52 Page:534-542
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Guy John,Qi Xiaoping,Pallotti Francesco,Schon Eric A.,Manfredi Giovanni,Carelli Valerio,Martinuzzi Andrea,Hauswirth William W.,Lewin Alfred S.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference41 articles.

1. Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy

2. Protein Sorting to Mitochondria: Evolutionary Conservations of Folding and Assembly

3. Mitochondrial genetics and disease

4. The epidemiology of pathogenic mitochondrial DNA mutations

5. Biochemical features of mtDNA 14484 (ND6/m64V) point mutation associated with Leber's hereditary optic neuropathy

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1. Hormonal orchestra: mastering mitochondria's role in health and disease;Endocrine;2024-08-22

2. Gene therapy for Leber hereditary optic neuropathy;Expert Opinion on Biological Therapy;2024-06-02

3. Galactose-replacement unmasks the biochemical consequences of the G11778A mitochondrial DNA mutation of LHON in patient-derived fibroblasts;Experimental Cell Research;2024-06

4. Development of mitochondrial gene-editing strategies and their potential applications in mitochondrial hereditary diseases: a review;Cytotherapy;2024-01

5. Leber hereditary optic neuropathy gene therapy;Current Opinion in Ophthalmology;2023-12-21

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