F. Zafarghandi Motlagh

Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect

S. Zeinali, A. Surguchov, Y. Nilipour, 2019, Molecular genetics & genomic medicine.

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.

Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort

S. Zeinali, M. Abiri, M. Hashemi, 2018, Metabolic Brain 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.