Severe Molecular Defects of a NovelFOXC1 W152GMutation Result in Aniridia-Reference-Cited by-同舟云学术

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Severe Molecular Defects of a NovelFOXC1 W152GMutation Result in Aniridia

Published:2009-08-01 Issue:8 Volume:50 Page:3573
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Ito Yoko A.¹,Footz Tim K.¹,Berry Fred B.¹,Mirzayans Farideh¹,Yu May¹,Khan Arif O.²,Walter Michael A.³

Affiliation:

1. From the Departments of Medical Genetics and

2. Pediatric Ophthalmology Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

3. From the Departments of Medical Genetics and3Ophthalmology, University of Alberta, Edmonton, AB, Canada; and the

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

Cited by 43 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Anterior segment dysgenesis: part II—genetics and pathogenesis;Expert Review of Ophthalmology;2024-03-05

2. Genetic changes and testing associated with childhood glaucoma: A systematic review;PLOS ONE;2024-02-22

3. Genetics of Childhood Glaucoma;Childhood Glaucoma;2024

4. Genetic Analysis by NGS and MLPA in Chinese Aniridia Patients;2023-08-16

5. Oncogenic Mutations in the DNA-Binding Domain of FOXO1 that Disrupt Folding: Quantitative Insights from Experiments and Molecular Simulations;Biochemistry;2022-07-27

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