Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

Abstract Purpose: To estimate carrier frequencies of CYP1B1 mutations p.Gly61Glu and p.Arg368His, respectively, in Talesh and the east of Guilan province in Iran with a maximum error of 2%. Previously, it was shown that these CYP1B1 mutations may be relatively prevalent in these regions. Methods: Po...

Full description

Bibliographic Details
Main Authors: Ali Heshmati, Peyman Taghizadeh, Hamid Ahmadieh, Mehdi Yaseri, Fatemeh Suri, Mahsa Alizadeh, Marjan Dadashzadeh, Hajar Khatami, Monireh Moradkhah Navi, Parisa Zamanparvar, Hassan Behboudi, Elahe Elahi
Format: Article
Language:English
Published: Knowledge E 2021-10-01
Series:Journal of Ophthalmic & Vision Research
Subjects:
cyp1b1
guilan
iran
p.arg368his
p.gly61glu
primary congenital glaucoma
Online Access:https://doi.org/10.18502/jovr.v16i4.9747

Internet

https://doi.org/10.18502/jovr.v16i4.9747

Similar Items