In Vivo Assessment of Retinal Phenotypes in Axenfeld–Rieger Syndrome-Reference-Cited by-同舟云学术

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In Vivo Assessment of Retinal Phenotypes in Axenfeld–Rieger Syndrome

Published:2024-04-08 Issue:4 Volume:65 Page:20
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Untaroiu Ana¹,Reis Linda M.¹,Higgins Brian P.¹,Walesa Ashleigh¹,Zacharias Serena²,Nikezic Danica¹,Costakos Deborah M.¹,Carroll Joseph¹³,Semina Elena V.¹³⁴

Affiliation:

1. Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, United States

2. School of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin, United States

3. Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, Wisconsin, United States

4. Department of Pediatrics and Children's Research Institute, Medical College of Wisconsin and Childrens Wisconsin, Milwaukee, Wisconsin, United States

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Reference56 articles.

1. Axenfeld-Rieger syndrome: more than meets the eye;Reis;J Med Genet,2023

2. Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants;Souzeau;Eur J Hum Genet,2017

3. FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma;Or;Exp Eye Res,2020

4. Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations;Weisschuh;Invest Ophthalmol Vis Sci,2006

5. Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome;Zhou;Exp Eye Res,2023

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