Detection of extremely low levels of wild-type mitochondrial DNA in the liver of a patient with pearson syndrome by a sensitive PCR assay
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF02435963
Reference13 articles.
1. Anderson S, Bankier AT, Barrel BG et al (1981) Sequence and organization of the human mitochondrial genome.Nature 290: 457–465.
2. Cormier V, Rötig A, Quartino AR et al (1990) Widespread multitissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome.J Pediatr 117: 599–602.
3. Holt IJ, Harding AE, Morgan-Hughes JA (1988) Deletions of mitochondrial DNA in patients with mitochondrial myopathies.Nature 331: 717–719.
4. Holt IJ, Harding AE, Cooper JM et al (1989) Mitochondrial myopathies: clinical and biochemical features in 30 cases with deletions of muscle mitochondrial DNA.Ann Neurol 26: 699–708.
5. Larsson N, Holme E, Kristiansson B, Oldfors A, Tulinius M (1990) Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.Pediatr Res 28: 131–136.
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