Progressive external ophthalmoplegia: A new family with tremor and peripheral neuropathy
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference9 articles.
1. Clinical and Genetic Heterogeneity in Progressive External Ophthalmoplegia Due to Mutations in Polymerase γ
2. Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance
3. Mutations of mitochondrial DNA polymerase ?A are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia
4. Active Site Mutation in DNA Polymerase γ Associated with Progressive External Ophthalmoplegia Causes Error-prone DNA Synthesis
5. Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria
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