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Multiple sclerosis and mitochondrial gene variations: A review

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Date
2013
Author
Andalib, S
Talebi, M
Sakhinia, E
Farhoudi, M
Sadeghi-Bazargani, H
Motavallian, A
Pilehvar-Soltanahmadi, Y
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Abstract
Multiple sclerosis (MS) is a debilitating disease of the central nervous system. Its etiology is still an unanswered enigma; its symptoms are varied and unpredictable; and there is no cure for it Genetics has been introduced as a contributing factor to MS. Not only may MS stem from nuclear gene variations/mutations, but also it may arise from mitochondrial gene variations/mutations. The association of mitochondrial DNA variations/mutations with the pathogenesis of MS has, so far, been analyzed by several studies. This paper reviews the literature with regard to MS and corresponding mitochondrial DNA variations. (C) 2013 Elsevier B.V. All rights reserved.
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http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/49139
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