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Ophthalmic Genetics Volume 36, 2015 - Issue 1
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Letter to the Journal

A Novel CYP1B1 Mutation with Congenital Glaucoma and Total Aniridia

Sultan AlzuhairyKing Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia,
,
Khaled K. Abu-AmeroDepartment of Ophthalmology, King Saud University, Riyadh, Kingdom of Saudi Arabia, and
,
Sami Al-ShahwanKing Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia,
&
Deepak P. EdwardKing Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia, ;Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore Maryland, USACorrespondence[email protected]
Pages 89-91 | Received 30 May 2013, Accepted 26 Jul 2013, Published online: 03 Sep 2013

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Read on this site (1)

Monica Samant, Bharesh K. Chauhan, Kira L. Lathrop & Ken K. Nischal. (2016) Congenital aniridia: etiology, manifestations and management. Expert Review of Ophthalmology 11:2, pages 135-144.
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Articles from other publishers (4)

Sucheta Parija & Saswati Sen. (2022) Childhood glaucoma – A review of basics. Medical Journal of Dr. D.Y. Patil Vidyapeeth 15:2, pages 148.
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Susana Alexandre-Moreno, Juan-Manuel Bonet-Fernández, Raquel Atienzar-Aroca, José-Daniel Aroca-Aguilar & Julio Escribano. (2021) Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes. International Journal of Molecular Sciences 22:12, pages 6430.
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Hyun Taek Lim, Dae Hee Kim & Hyuna Kim. (2017) PAX6 aniridia syndrome. Current Opinion in Ophthalmology 28:5, pages 436-447.
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Carly J. Lewis, Adam Hedberg-Buenz, Adam P. DeLuca, Edwin M. Stone, Wallace L.M. Alward & John H. Fingert. (2017) Primary congenital and developmental glaucomas. Human Molecular Genetics 26:R1, pages R28-R36.
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