CYP1B1 Cytopathy: Uncommon Phenotype of a Homozygous CYP1B1 Deletion as Internal Corneal Ulcer of Von Hippel

Author:

Oliva-Biénzobas Valeria,Navas Alejandro,C. Astiazarán Mirena,Chacón-Camacho Oscar Francisco,A. Bermúdez-Magner Jose,Takane Mariana,Graue-Hernández Enrique,Zenteno Juan Carlos

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology

Reference11 articles.

1. Genetics of congenital corneal opacification—Impact on diagnosis and treatment;Nischal;Cornea,2015

2. Congenital corneal opacities;Cotran;Int Ophthalmol Clin.,1992

3. Null CYP1B1 Genotypes in primary congenital and Nondominant juvenile glaucoma;López-Garrido;Ophthalmology,2012

4. Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly;Vincent;J Med Genet.,2001

5. Primary congenital glaucoma and Rieger's anomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations;Chavarria-Soley;Mol Vis.,2006

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