Muscle mitochondrial DNA in encephalomyopathy and ragged red fibres: a Southern blot analysis and literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/content/pdf/10.1007/BF00319685.pdf
Reference67 articles.
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1. Chapter 2 Clinical Features of the Mitochondrial Encephalomyopathies;Mitochondrial Disorders in Neurology 2;2002
2. Mitochondrial Encephalomyopathy and Hypoparathyrodism Associated with a Duplication and a Deletion of Mitochondrial Deoxyribonucleic Acid;Journal of Clinical Endocrinology & Metabolism;1998-01-01
3. Mitochondrial disorders in degenerative ataxias;European Journal of Neurology;1996-01
4. Mitochondrial myopathies: clinical features, investigation, treatment and genetic counselling;Mitochondrial Disorders in Neurology;1994
5. Mitochondrial DNA Deletion in Kearns-Sayre Syndrome: A Review and Illustration of Cases;Annals of Saudi Medicine;1993-03
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