Corneal ectasia in a boy with homozygous KERA mutation-Reference-Cited by-同舟云学术

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Corneal ectasia in a boy with homozygous KERA mutation

Published:2017-08-11 Issue:1 Volume:39 Page:141-143
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Khan Arif O.¹

Affiliation:

1. Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2017.1350724

Reference13 articles.

1. Mutations in KERA, encoding keratocan, cause cornea plana

2. Recessive Cornea Plana in the Kingdom of Saudi Arabia

3. Axial Lengths in Children with Recessive Cornea Plana

4. Structure and Sequence of the Gene Encoding Human Keratocan

5. HGMD Mutation Result [Internet]. [accessed 2017 May 6]. http://www.hgmd.cf.ac.uk/ac/all.php.

Cited by 4 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. Cornea and Sclera;Ocular Pathology;2025

2. Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms;Progress in Retinal and Eye Research;2024-09

3. Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans;Journal of Cell Communication and Signaling;2021-04-15

4. Novel variants in the KERA gene cause autosomal recessive cornea plana in a Chinese family: A case report;Molecular Medicine Reports;2019-04-11

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