Ocular Manifestations and Histologic Characteristics of Keratitis-Ichthyosis-Deafness (KID) Syndrome
Author:
Affiliation:
1. Department of Ophthalmology, Chung-Ang University Yongsan Hospital, Seoul, Korea.
2. Modern Cell & Tissue Technologies, Seoul, Korea.
Publisher
Korean Ophthalmological Society
Subject
Ophthalmology
Link
https://synapse.koreamed.org/pdf/10.3341/jkos.2008.49.9.1532
Reference23 articles.
1. The Keratitis, Ichthyosis, and Deafness (KID) Syndrome
2. De novo mutation in the gene encoding connexin-26 (GJB2) in a sporadic case of keratitis-ichthyosis-deafness (KID) syndrome
3. Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome
4. Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome
5. A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
Cited by 1 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 Manifestations, Treatment Outcome and Clinical Course of Infective Keratitis of Keratitis-Ichthyosis-Deafness Syndrome;Journal of the Korean Ophthalmological Society;2019
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