Mitochondrial diseases
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical)
Reference145 articles.
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2. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy;Wallace;Science,1988
3. Mitochondrial encephalomyopathies: gene mutation;Servidei;Neuromusc Disord,2000
4. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981
5. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA;Andreu;New Engl J Med,1999
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3. Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient rat model of a genetic mitochondrial DNA depletion syndrome;FREE RADICAL BIO MED;2016
4. Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment;Molecular Syndromology;2016
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