Case Series of Patients With Hereditary Benign Intraepithelial Dyskeratosis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology
Reference5 articles.
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2. A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis;Allingham;Am J Hum Genet.,2001
3. Corneal manifestations of hereditary benign intraepithelial dyskeratosis;Reed;Arch Ophthalmol.,1979
4. Discheratosi intraepiteliale benigna ereditaria. Studio di un nucleo familiare [Benign hereditary intraepithelial dyskeratosis. Study of a family nucleus];Gombos;G Ital Dermatol Venereol.,1986
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Cited by 2 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. Autoinflammatory Keratinization Diseases—The Concept, Pathophysiology, and Clinical Implications;Clinical Reviews in Allergy & Immunology;2023-12-16
2. Regarding Treatment and Features of a Case Series of Patients With Hereditary Benign Intraepithelial Dyskeratosis;Cornea;2022-11-21
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