Feyzollah Hashemi-Gorji

Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

V. Yassaee, M. Miryounesi, M. Fardaei, 2018, Molecular vision.

Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1.

V. Yassaee, N. Parvaneh, Sara Boosaliki, 2016, Human immunology.

A Novel Splice Site Mutation in HPS1 Gene is Associated with Hermansky-Pudlak Syndrome-1 (HPS1) in an Iranian Family

V. Yassaee, M. Miryounesi, S. Ghafouri-Fard, 2016, International journal of molecular and cellular medicine.

Neurodegeneration with brain iron accumulation 2A: Report of four independent cases

V. Yassaee, M. Miryounesi, Farzad Hashemi-Gorji, 2018 .