The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population
Nejat Mahdieh,
Morteza Heidari,
Zahra Rezaei
et al.
Abstract:Background
To investigate the genetics of early-onset progressive cerebellar ataxia in Iran, we conducted a study at the Children’s Medical Center (CMC), the primary referral center for pediatric disorders in the country, over a three-year period from 2019 to 2022. In this report, we provide the initial findings from the national registry.
Methods
We selected all early-onset patients with an autosomal recessive mode of inheritance to assess their p… Show more
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