T. Shirzadeh

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations

S. Zeinali, M. Abiri, Z. Salehi, 2019, Orphanet Journal of Rare Diseases.

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population

M. Alaei, S. Zeinali, M. Abiri, 2018, Journal of Inherited Metabolic Disease.

Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decade

M. Kabiri, S. Zeinali, A. Karimi, 2023, Frontiers in Genetics.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.