Maghsood Mehri

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.

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.

Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2022, Archives of Iranian medicine.

The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran

H. Najmabadi, A. Azarkeivan, M. Neishabury, 2021, Journal of Clinical Immunology.