نتایج جستجو برای: a12308g

تعداد نتایج: 11  

Journal: :iranian journal of child neurology 0
mohammad medhi heidari phd, assistant professor of molecular genetics, department of biology,sciences school,yazd university of medical sciences, yazd,iran mehri khatami phd, assistant professor of molecular genetics, department of biology,sciences school,yazd university of medical sciences, yazd,iran massoud houshmand phd, assistant professor of human molecular genetics,department of medical genetic,national institute of genetic engineering and biotechnology,tehran,iran eisa mahmoudi phd, assitant professor of mathematical statistic,department of statistics,yazd university, yazd,iran shahriar nafissi md, associate professor of neurology, neurology department, tehran university of medical sciences, tehran,iran

how to cite this article: heidari mm, khatami m, houshmand m, mahmoudi e, nafissi sh .increased prevalence 12308 a > g mutation in mitochondrialtrnaleu (cun) gene associated with earlier age of onset in friedreich ataxia. iranian journal of child neurology 2011;5(4):25-31. objective friedreich ataxia (frda) is an inherited recessive disorder. mitochondrial dna is a candidate modifying factor fo...

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