Novel Mitochondrial Homoplasmic T4216C Mutation in Iranian Patients with Friedreich Ataxia
Introduction: The mitochondrial defects in Friedreich ataxia (FRDA) have been reported in many researches. Friedreich ataxia is an autosomal recessive neurodegenerative disorder caused by decreased expression of the Frataxin protein. Frataxin deficiency leads to excessive free radical production and...
| Main Authors: | , |
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| Format: | Article |
| Language: | fas |
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Shahid Sadoughi University of Medical Sciences
2010-06-01
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| Series: | Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd |
| Subjects: | |
| Online Access: | http://85.185.157.11:6280/jssu/browse.php?a_id=1031&slc_lang=en&sid=1&ftxt=1 |