Next-generation sequencing approach to molecular diagnosis of Iranian patients with Duchenne/Becker muscular dystrophy: Several novel variants identified

por Bakhshandeh, MohammadKazem, Behroozi, Samira
Publicado 2023

A novel recessive PDZD7 bi-allelic mutation in an Iranian family with non-syndromic hearing loss

por Fahimi, Hossein, Behroozi, Samira, Noavar, Sadaf, Parvini, Farshid
Publicado 2021

A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature

por Noavar, Sadaf, Behroozi, Samira, Tatarcheh, Taraneh, Parvini, Farshid, Foroutan, Majid, Fahimi, Hossein
Publicado 2019