Long-Term Outcome After Penetrating Keratoplasty in a Pedigree With the G177E Mutation in the UBIAD1 Gene for Schnyder Corneal Dystrophy-Reference-Cited by-同舟云学术

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Long-Term Outcome After Penetrating Keratoplasty in a Pedigree With the G177E Mutation in the UBIAD1 Gene for Schnyder Corneal Dystrophy

Published:2018-01-09 Issue:5 Volume:37 Page:554-559
ISSN:0277-3740
Container-title:Cornea
language:en
Short-container-title:

Author:

Kitazawa Koji,Wakimasu Koichi,Kayukawa Kanae,Sugimoto Manabu,Nakai Junko,Weiss Jayne S.,Ueno Morio,Sotozono Chie,Kinoshita Shigeru

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology

Reference26 articles.

1. Schnyder dystrophy of the cornea. A Swede-Finn connection;Weiss;Cornea,1992

2. IC3D classification of corneal dystrophies–edition 2;Weiss;Cornea,2015

3. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy;Orr;PLoS One,2007

4. Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy;Weiss;Invest Ophthalmol Vis Sci.,2007

5. Identification of UBIAD1 as a novel human menaquinone-4 biosynthetic enzyme;Nakagawa;Nature,2010

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1. Management of Stromal Corneal Dystrophies; Review of the Literature with a Focus on Phototherapeutic Keratectomy and Keratoplasty;Vision;2023-03-13

2. Corneal Dysgeneses, Dystrophies, and Degenerations;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

3. Corneal Manifestations of Metabolic Disease;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

4. Functional study of SCCD pathogenic gene UBIAD1 (Review);Molecular Medicine Reports;2021-08-06

5. Interhelical H-Bonds Modulate the Activity of a Polytopic Transmembrane Kinase;Biomolecules;2021-06-25

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