Article ID Journal Published Year Pages File Type
8399225 Mitochondrion 2015 6 Pages PDF
Abstract
Urine cells had the highest mutation load for all of the mtDNA mutations studied. The mutation loads in the blood, urine and the buccal mucosa were significantly higher in the mitochondrial disorder group that manifested clinical signs than in the asymptomatic subjects. In conclusion, urine is a suitable biological sample for molecular diagnosis of mtDNA mutations and for the study of the attendant risk of recurrence in the offspring of asymptomatic mothers identified as non-carriers after mutation analysis in blood.
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Life Sciences Biochemistry, Genetics and Molecular Biology Biophysics
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