Repository of Research and Investigative Information
Shahid Sadoughi University of Medical Sciences
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(2024) The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population. Human Genomics. p. 18. ISSN 1473-9542
(2023) The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy. Journal of Neuromuscular Diseases. pp. 211-225. ISSN 2214-3599
(2017) <i>B3GALNT2</i> mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies. Genome medicine. p. 11. ISSN 1756-994X