CYP1B1 Mutation Profile of Iranian Primary Congenital Glaucoma Patients and Associated Haplotypes
โ Scribed by Chitsazian, Fereshteh; Tusi, Betsabeh Khoramian; Elahi, Elahe; Saroei, Heidar Amini; Sanati, Mohammad H.; Yazdani, Shahin; Pakravan, Mohammad; Nilforooshan, Navid; Eslami, Yadollah; Mehrjerdi, Mohammad Ali Zare; Zareei, Reza; Jabbarvand, Mahmood; Abdolahi, Ali; Lasheyee, Ali R.; Etemadi, Arash; Bayat, Behnaz; Sadeghi, Mehdi; Banoei, Mohammad M.; Ghafarzadeh, Behnam; Rohani, Mohammad R.; Rismanchian, Akram; Thorstenson, Yvonne; Sarfarazi, Mansoor
- Book ID
- 120773714
- Publisher
- American Society for Investigative Pathology
- Year
- 2007
- Tongue
- English
- Weight
- 307 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1525-1578
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๐ SIMILAR VOLUMES
The CYP1B1 gene (GenBank: U56438), a member of the cytochrome P450 gene family, has been shown to be mutated in patients with primary congenital glaucoma (PCG), a rare but severely blinding form of glaucoma. Here, we have investigated CYP1B1 mutations in 31 unrelated French PCG patients. Mutations w