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

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: Population-...

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Detalles Bibliográficos
Autores principales: Heshmati, Ali, Taghizadeh, Peyman, Ahmadieh, Hamid, Yaseri, Mehdi, Suri, Fatemeh, Alizadeh, Mahsa, Dadashzadeh, Marjan, Khatami, Hajar, Navi, Monireh Moradkhah, Zamanparvar, Parisa, Behboudi, Hassan, Elahi, Elahe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PUBLISHED BY KNOWLEDGE E 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593531/
https://www.ncbi.nlm.nih.gov/pubmed/34840680
http://dx.doi.org/10.18502/jovr.v16i4.9747

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593531/
https://www.ncbi.nlm.nih.gov/pubmed/34840680
http://dx.doi.org/10.18502/jovr.v16i4.9747

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