The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/124/1/209/806351/1240209.pdf
Reference44 articles.
1. Sequence and organization of the human mitochondrial genome
2. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
3. The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme
4. Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene
5. The enigmatic relationship between mitochondrial dysfunction and Leber’s hereditary optic neuropathy
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