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CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
Chitsazian F, Tusi BK, Elahi E, Saroei HA, Sanati MH, Yazdani S, Pakravan M, Nilforooshan N, Eslami Y, Mehrjerdi MA, Zareei R, Jabbarvand M, Abdolahi A, Lasheyee AR, Etemadi A, Bayat B, Sadeghi M, Banoei MM, Ghafarzadeh B, Rohani MR, Rismanchian A, Thorstenson Y, Sarfarazi M. Chitsazian F, et al. Among authors: elahi e. J Mol Diagn. 2007 Jul;9(3):382-93. doi: 10.2353/jmoldx.2007.060157. J Mol Diagn. 2007. PMID: 17591938 Free PMC article.
Contributions of MYOC and CYP1B1 mutations to JOAG.
Bayat B, Yazdani S, Alavi A, Chiani M, Chitsazian F, Tusi BK, Suri F, Narooie-Nejhad M, Sanati MH, Elahi E. Bayat B, et al. Among authors: elahi e. Mol Vis. 2008 Mar 13;14:508-17. Mol Vis. 2008. PMID: 18385784 Free PMC article.
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma.
Narooie-Nejad M, Paylakhi SH, Shojaee S, Fazlali Z, Rezaei Kanavi M, Nilforushan N, Yazdani S, Babrzadeh F, Suri F, Ronaghi M, Elahi E, Paisán-Ruiz C. Narooie-Nejad M, et al. Among authors: elahi e. Hum Mol Genet. 2009 Oct 15;18(20):3969-77. doi: 10.1093/hmg/ddp338. Epub 2009 Aug 4. Hum Mol Genet. 2009. PMID: 19656777
204 results