Article
Graded gene expression changes determine phenotype severity in mouse models of CRX-associated retinopathies.
Genome biology - 1 Sept 2015
Ruzycki Philip A, Tran Nicholas M, Kefalov Vladimir J, Kolesnikov Alexander V, Chen Shiming
Abstract excerpt
BACKGROUND: Mutations in the cone-rod-homeobox protein CRX are typically associated with dominant blinding retinopathies with variable age of onset and severity. Five well-characterized mouse models carrying different Crx mutations show a wide range of disease phenotypes. To determine if the phen...
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