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Brain & Development|December 21, 2023
A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophiesSareh Hosseinpour, Ehsan Razmara, Morteza Heidari, et al.Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.Brain : a Journal of Neurology|February 22, 2024
ZSCAN10 deficiency causes a neurodevelopmental disorder with characteristic oto-facial malformationsLucia Laugwitz, Fubo Cheng, Stephan C Collins, et al.Pageof 19