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Items: 3

1.
A mouse model of brittle cornea syndrome caused by mutation in Zfp469
Chloe M. Stanton, Amy S. Findlay, Camilla Drake, Mohammad Z. Mustafa, Philippe Gautier, Lisa McKie, Ian J. Jackson, Veronique Vitart
Dis Model Mech. 2021 Sep 1; 14(9): dmm049175. Published online 2021 Sep 22. doi: 10.1242/dmm.049175
PMCID:
PMC8476817
AbstractArticle
2.
Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus
Judith Lechner, Louise F. Porter, Aine Rice, Veronique Vitart, David J. Armstrong, Daniel F. Schorderet, Francis L. Munier, Alan F. Wright, Chris F. Inglehearn, Graeme C. Black, David A. Simpson, Forbes Manson, Colin E. Willoughby
Hum Mol Genet. 2014 Oct 15; 23(20): 5527–5535. Published online 2014 Jun 3. doi: 10.1093/hmg/ddu253
PMCID:
PMC4168824
AbstractArticlePDF–500K
3.
Defects in retinal pigment epithelium cell proliferation and retinal attachment in mutant mice with p27Kip1 gene ablation
Dennis M. Defoe, Lorrie B. S. Adams, Jingru Sun, Sarah N. Wisecarver, Edward M. Levine
Mol Vis. 2007; 13: 273–286. Published online 2007 Feb 27.
PMCID:
PMC2633469
AbstractArticlePDF–1.2M

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