[1]
HEIDARI*, M.M., KHATAMI, M. and POURAKRAMI, J. 2014. Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich’s Ataxia. Iranian Journal of Child Neurology. 8, 1 (Jan. 2014), 32–36. DOI:https://doi.org/10.22037/ijcn.v8i1.4115.