M. Mehri

Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes

H. Najmabadi, Z. Fattahi, A. Azarkeivan, 2020, Haematologica.

Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing.

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2018, Blood cells, molecules & diseases.