Items where Author is "Hejazifar, A."

Article

(2021) Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature. J Hum Genet. ISSN 1434-5161

(2021) Identification of a Missense Variant in the EIF2B3 Gene Causing Vanishing White Matter Disease with Antenatal-Onset but Mild Symptoms and Long-Term Survival. J Mol Neurosci. ISSN 0895-8696

(2019) Targeted next generation sequencing reveals genetic defects underlying inherited retinal disease in Iranian families. Molecular Vision. pp. 106-117. ISSN 1090-0535