Homozygotic Patient with βig-h3 Gene Mutation in Granular Dystrophy-Reference-Cited by-同舟云学术

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Homozygotic Patient with βig-h3 Gene Mutation in Granular Dystrophy

Published:1998-05 Issue:3 Volume:17 Page:288-292
ISSN:0277-3740
Container-title:Cornea
language:en
Short-container-title:Cornea

Author:

Fujiki Keiko,Hotta Yoshihiro,Nakayasu Kiyoo,Kanai Atsushi

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology

Cited by 39 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. Ocular genetics in the Japanese population;Japanese Journal of Ophthalmology;2024-09-14

2. Genotypic Homogeneity in Distinctive Transforming Growth Factor-Beta Induced (TGFBI) Protein Phenotypes;International Journal of Molecular Sciences;2021-01-27

3. Multiple excimer laser phototherapeutic keratectomies for Avellino corneal dystrophy: a case report;International Journal of Ophthalmology;2020-05-18

4. Cornea guttata associated with special phenotypic variants of granular corneal dystrophy type 2 in a Chinese family;European Journal of Ophthalmology;2019-03-14

5. Simultaneous Transplantation of Limbal Stem Cells May Reduce Recurrences of Granular Dystrophy After Corneal Transplantation;Medicine;2015-05

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