Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosa

被引：0
|
作者：
Danial Roshandel
Maryam Rafati
Sara Khorami
Nima Novin Baheran
Setareh Jalali
Razieh Tabatabaie
Safura Rezai
Hamid Ahmadieh
Saeed Reza Ghaffari
机构：
[1] Shahid Beheshti University of Medical Sciences,Ocular Tissue Engineering Research Center
[2] ACECR,Reproductive Biotechnology Research Center, Avicenna Research Institute
[3] Hope Generation Foundation,Fetal Health Research Center
[4] Gene Clinic,Ophthalmic Research Center
[5] Shahid Beheshti University of Medical Sciences,undefined
来源：
International Ophthalmology | 2019年 / 39卷
关键词：
Retinitis pigmentosa; Rhodopsin; Mutation; Genotype–phenotype correlation;
D O I：
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学科分类号：
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页码：2523 / 2531
页数：8
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