Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa

por Bushehri, Ata, Zare-Abdollahi, Davood, Alavi, Afagh, Dehghani, Alireza, Mousavimikala, Mohammadreza, Khorram Khorshid, Hamid Reza
Publicado 2019

Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia

por Bushehri, Ata, Zare-Abdollahi, Davood, Hashemian, Hesam, Safavizadeh, Ladan, Effati, Jalil, Khorram Khorshid, Hamid Reza
Publicado 2020

Identification of a Novel Homozygous Mutation in BBS10 Gene in an Iranian Family with Bardet-Biedl Syndrome

por Dehani, Mohammad, Zare-Abdollahi, Davood, Bushehri, Ata, Dehghani, Azadeh, Effati, Jalil, Miratashi, Seyed Ali Mohammad, Khorram Khorshid, Hamid Reza
Publicado 2021