The First Report of Iranian Registry of Patients with Spinal Muscular AtrophyVahid Mansouri, Mahmoud Reza Ashrafi, Reza Shervin Badv et al.|Journal of Neuromuscular Diseases|2023Cited by 14
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoud Reza Ashrafi, Masoud Garshasbi, Reyhaneh Kameli et al.|Neurogenetics|2023Cited by 4
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoud Reza Ashrafi, Masoud Garshasbi, Reyhaneh Kameli et al.|Neurogenetics|2023Cited by 0
A de novo start-loss variant in the NIPBL gene causing mild type 1 Cornelia de Lange syndrome in an Iranian family: A Case ReportAtefeh Mir, MohammadAmin Tabatabaiefar, Zahra Abbasi et al.|Journal of Medical Case Reports|2026Cited by 0