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6 in total

Review 1. Mitochondrial DNA and genetic disease.

Authors: J Poulton
Journal: Arch Dis Child Date: 1988-08 Impact factor: 3.791

2. Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatment.

Authors: F A Wijburg; P G Barth; W Ruitenbeek; R J Wanders; G D Vos; S L Ploos van Amstel; R B Schutgens
Journal: J Inherit Metab Dis Date: 1989 Impact factor: 4.982

3. Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase.

Authors: A Chomyn; P Mariottini; M W Cleeter; C I Ragan; A Matsuno-Yagi; Y Hatefi; R F Doolittle; G Attardi
Journal: Nature Date: 1985 Apr 18-24 Impact factor: 49.962

4. High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells.

Authors: E Ching; G Attardi
Journal: Biochemistry Date: 1982-06-22 Impact factor: 3.162

5. Mitochondrial inheritance in a mitochondrially mediated disease.

Authors: J Egger; J Wilson
Journal: N Engl J Med Date: 1983-07-21 Impact factor: 91.245

6. Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

Authors: H S Rosing; L C Hopkins; D C Wallace; C M Epstein; K Weidenheim
Journal: Ann Neurol Date: 1985-03 Impact factor: 10.422

6 in total