Sequence analysis of familial PEO shows additional mutations associated with the 752C?T and 3527C?T changes in thePOLG1 gene
- 31 August 2004
- journal article
- Published by Wiley in Annals of Neurology
- Vol. 56 (3) , 454-455
- https://doi.org/10.1002/ana.20219
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsHuman Mutation, 2003
- Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathyEuropean Journal of Human Genetics, 2003
- Mutations of ANT1 , Twinkle , and POLG1 in sporadic progressive external ophthalmoplegia (PEO)Neurology, 2003
- Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaAnnals of Neurology, 2002