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...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: 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
Langue:EN
Publié: Knowledge E 2021
Sujets:
Accès en ligne:https://doaj.org/article/b4b18880fe45485489ffda447c4f575e
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!