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2001 | 42 | 3 | 351-358
Article title

MELAS as an example of a mitochondrial disease

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EN
Abstracts
EN
MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) is a disease mainly due to a mutation at position 3243 (A G) in the leucine tRNA gene in mitochondrial DNA. Symptoms of the disorder are complex and the exact pathogenesis is not understood. A review of the literature on the subject is presented.
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Year
Volume
42
Issue
3
Pages
351-358
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Document Type
REVIEW
Publication order reference
E. Bartnik, Department of Genetics, University of Warsaw and Institute of Biochemistry and Biophysics, Polish Academy of Sciences, ul. Pawinskiego 5a, 02-106 Warszawa, Poland, e-mail: ebartnik@ibb.waw.pl
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YADDA identifier
bwmeta1.element.element-from-psjc-73237619-e518-39c6-a847-a2ae26f67386
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