Oxidative Phosphorylation Disease Diagnosis
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1999.tb07817.x/fullpdf
Reference97 articles.
1. 1Shoffner, J.M. & D.C. Wallace. 1995. Oxidative phosphorylation diseases.InThe Metabolic and Molecular Bases of Inherited Disease: 1535-1610.
2. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
3. Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution
4. Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form
5. Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA
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