Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8399225 | Mitochondrion | 2015 | 6 Pages |
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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Authors
MarÃa M. O'Callaghan, Sonia Emperador, Mercè Pineda, Ester López-Gallardo, Raquel Montero, Delia Yubero, Cristina Jou, Cecilia Jimenez-Mallebrera, Andrés Nascimento, Isidre Ferrer, Angels GarcÃa-Cazorla, Eduardo Ruiz-Pesini, Julio Montoya,