Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA
Author:
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/128/8/1861/1301545/awh515.pdf
Reference31 articles.
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3. Brierley EJ, Johnson MA, Bowman A, Ford GA, Subhan F, Reed JW, et al. Mitochondrial function in muscle from elderly athletes. Ann Neurol1997; 41: 114–6.
4. Chinnery PF, Howell N, Lightowlers RN, Turnbull DM. Molecular pathology of MELAS and MERFF. The relationship between mutation load and clinical phenotypes. Brain1997; 120: 1713–21.
5. Chinnery PF, Howel D, Turnbull DM, Johnson MA. Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibers. J Neurol Sci2003; 211: 63–6.
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