Neurodegenerative parkinsonism and progressive external ophthalmoplegia with a Twinkle mutation
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference7 articles.
1. Expanding insights into mitochondrial dysfunction in Parkinson's disease;Abou-Sleiman;Nat Rev Neurosci,2006
2. Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study;Luoma;Lancet,2004
3. Reconstitution of a minimal mtDNA replisome in vitro;Korhonen;EMBO J,2004
4. Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria;Spelbrink;Nat Genet,2001
5. Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase Twinkle;Baloh;Arch Neurol,2007
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