Functional Analysis of Lymphoblast and Cybrid Mitochondria Containing the 3460, 11778, or 14484 Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation-Reference-Cited by-同舟云学术

Functional Analysis of Lymphoblast and Cybrid Mitochondria Containing the 3460, 11778, or 14484 Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation

Published:2000-12 Issue:51 Volume:275 Page:39831-39836
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Brown Michael D.,Trounce Ian A.,Jun Albert S.,Allen Jon C.,Wallace Douglas C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference27 articles.

1. Leber hereditary optic neuropathy: Mitochondrial mutations and degeneration of the optic nerve

2. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

3. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees.

4. A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.

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