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

Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular Dystrophy

por KHODAENIA, Negar, FARJAMI, Zahra, ASHNAEI, Amir Hosein, EBRAHIMI, Neshat, CHELVARFOROOSH, Navid, URTIZBEREA, Andoni, RAZMARA, Ehsan, HOUSHMAND, Massoud
Publicado 2021