Mohammad Farid Mohammadi

Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome Sequencing

A. Tavasoli, Pouria Mohammadi, G. Zamani, 2022, Journal of Molecular Neuroscience.

Whole‐exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3

Navid Almadani, M. Garshasbi, Pouria Mohammadi, 2021, Molecular genetics & genomic medicine.

Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMT

Seyedeh-Atiyeh Afjei, A. Tavasoli, M. Ashrafi, 2023, neurogenetics.

Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature.

M. Garshasbi, A. Tavasoli, Pouria Mohammadi, 2023, Irish journal of medical science.

Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers

Seyed Mohammad Salar Zaheryani, M. Garshasbi, Pouria Mohammadi, 2023, Clinical case reports.