A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity)

por Torkamandi, Shahram, Rezaei, Somaye, Mirfakhraie, Reza, Bayat, Sahar, Piltan, Samira, Gholami, Milad
Publicado 2020

Ectopic expression of CYP24A1 circular RNA hsa_circ_0060927 in uterine leiomyomas

por Fazeli, Elnaz, Piltan, Samira, Sadeghi, Hossein, Gholami, Milad, Azizi‐Tabesh, Ghasem, Yassaee, Fakhrolmolook, Mirfakhraie, Reza
Publicado 2019