Evaluation of GKN1 and GKN2 gene expression as a biomarker of gastric cancer

por Dokhaee, Fatemeh, Mazhari, Sogol, Galehdari, Mohammad, Bahadori Monfared, Ayad, Baghaei, Kaveh
Publicado 2018

A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family

por Sepahvand, Afrooz, Razmara, Ehsan, Bitarafan, Fatemeh, Galehdari, Mohammad, Tavasoli, Ali Reza, Almadani, Navid, Garshasbi, Masoud
Publicado 2020

A case report of congenital myasthenic syndrome caused by a mutation in theCHRNE genein the Iranian population

por FARJAMI, Zahra, KHODAENIA, Negar, EBRAHIMI, Neshat, ZAMANI, Gholamreza, ASHNAEI, Amir Hosein, GALEHDARI, Mohammad, MORADYAR, Mehdi, HOUSHMAND, Massoud
Publicado 2020

Whole‐exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis

por Razmara, Ehsan, Azimi, Homeyra, Bitaraf, Amirreza, Daneshmand, Mohammad Ali, Galehdari, Mohammad, Dokhanchi, Maryam, Esmaeilzadeh‐Gharehdaghi, Elika, Garshasbi, Masoud
Publicado 2020