» Articles » PMID: 550801

Corneal Manifestations of Hereditary Benign Intraepithelial Dyskeratosis

Overview
Journal Arch Ophthalmol
Specialty Ophthalmology
Date 1979 Feb 1
PMID 550801
Citations 3
Authors
Affiliations
Soon will be listed here.
Citing Articles

Hereditary Benign Intraepithelial Dyskeratosis: Report of a Case and Re-examination of the Evidence for Locus Heterogeneity.

Bui T, Young J, Frausto R, Markello T, Glasgow B, Aldave A Ophthalmic Genet. 2014; 37(1):76-80.

PMID: 24555743 PMC: 4139474. DOI: 10.3109/13816810.2014.889169.


Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis.

Soler V, Tran-Viet K, Galiacy S, Limviphuvadh V, Klemm T, St Germain E J Med Genet. 2013; 50(4):246-54.

PMID: 23349227 PMC: 4115150. DOI: 10.1136/jmedgenet-2012-101325.


A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.

Allingham R, Seo B, Rampersaud E, Bembe M, Challa P, Liu N Am J Hum Genet. 2001; 68(2):491-4.

PMID: 11170897 PMC: 1235282. DOI: 10.1086/318194.