A Report of a Novel Mutation in Human Prostacyclin Receptor Gene in Patients Affected with Migraine

por Kheirollahi, Majid, Pourreza, Mohammad Reza, Khorvash, Fariborz, Kazemi, Mohammad, Amini, Gilda
Publicado 2017

Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper

por Pourreza, Mohammad Reza, Mohammadi, Hannane, Sadeghian, Ladan, Asgharzadeh, Samira, Sehhati, Mohammadreza, Tabatabaiefar, Mohammad Amin
Publicado 2018

Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation

por Ataei, Zahra, Nouri, Zahra, Tavakoli, Farial, Pourreza, Mohammad Reza, Narrei, Sina, Tabatabaiefar, Mohammad Amin
Publicado 2023

A pathogenic variant in the transforming growth factor beta I (TGFBI) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review

por Mohammadi, Aliasgar, Ahmadi Shadmehri, Azam, Taghavi, Mahnaz, Yaghoobi, Gholamhossein, Pourreza, Mohammad Reza, Tabatabaiefar, Mohammad Amin
Publicado 2020