Novel Missense Mitochondrial ND4L Gene Mutations in Friedreich's Ataxia
AbstractObjective(s)The mitochondrial defects in Friedreich's ataxia have been reported in many researches. Mitochondrial DNA is one of the candidates for defects in mitochondrion, and complex I is the first and one of the largest catalytic complexes of oxidative phosphorylation (OXPHOS) system...
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| Format: | Article |
| Language: | English |
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Mashhad University of Medical Sciences
2011-05-01
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| Series: | Iranian Journal of Basic Medical Sciences |
| Subjects: | |
| Online Access: | http://www.mums.ac.ir/shares/basic_medical/basicmedjou/2011/may/a4.pdf |