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Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma.
Ophthalmology. 2009 Nov;116(11):2101-9. doi: 10.1016/j.ophtha.2009.04.045. Epub 2009 Sep 10.
Ophthalmology. 2009.
PMID: 19744731
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: narooie nejhad m.
Mol Vis. 2008 Mar 13;14:508-17.
Mol Vis. 2008.
PMID: 18385784
Free PMC article.
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Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol.
Suri F, Kalhor R, Zargar SJ, Nilforooshan N, Yazdani S, Nezari H, Paylakhi SH, Narooie-Nejhad M, Bayat B, Sedaghati T, Ahmadian A, Elahi E.
Suri F, et al. Among authors: narooie nejhad m.
Mol Vis. 2008;14:2349-56. Epub 2008 Dec 18.
Mol Vis. 2008.
PMID: 19096718
Free PMC article.
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Myocilin mutations are not a major cause of primary congenital glaucoma in Iranian patients.
Elahi E, Narooie-Nejhad M, Suri F, Yazdani S.
Elahi E, et al. Among authors: narooie nejhad m.
J Ophthalmic Vis Res. 2010 Apr;5(2):101-4.
J Ophthalmic Vis Res. 2010.
PMID: 22737338
Free PMC article.
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