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Publications by Brent Higgins
Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy
PLoS ONE
Multidisciplinary
Related publications
Mutations in theUBIAD1Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Clinical Diversity in Patients With Schnyder Corneal Dystrophy—a Novel and Known UBIAD1 Pathogenic Variants
Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Schnyder Corneal Dystrophy-Associated UBIAD1 Is Defective in MK-4 Synthesis and Resists Autophagy-Mediated Degradation
Journal of Lipid Research
Biochemistry
Endocrinology
Cell Biology
Central Crystalline Corneal Dystrophy.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
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Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
American Journal of Human Genetics
Genetics
Hereditary Crystalline Stromal Dystrophy of Schnyder. I. Clinical Features of a Family With Hyperlipoproteinaemia.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
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Truncating Mutations in the Carbohydrate Sulfotransferase 6 Gene (CHST6) Result in Macular Corneal Dystrophy
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
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Mutations in the PCYT1A Gene Are Responsible for Isolated Forms of Retinal Dystrophy
European Journal of Human Genetics
Genetics
Advanced Corneal Imaging for Fuchs Endothelial Corneal Dystrophy
Ophthalmology
Ophthalmology
