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...

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Autores principales: 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
Formato: article
Lenguaje:EN
Publicado: Knowledge E 2021
Materias:
cyp1b1
guilan
iran
p.arg368his
p.gly61glu
primary congenital glaucoma
Ophthalmology
RE1-994
Acceso en línea:https://doaj.org/article/b4b18880fe45485489ffda447c4f575e
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https://doaj.org/article/b4b18880fe45485489ffda447c4f575e

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