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Publications by Muriel Kaiser-Kupfer
Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
American Journal of Human Genetics
Genetics
Related publications
Identification and Population History of CYP4V2 Mutations in Patients With Bietti Crystalline Corneoretinal Dystrophy
European Journal of Human Genetics
Genetics
Detailed Functional and Structural Phenotype of Bietti Crystalline Dystrophy Associated With Mutations in CYP4V2 Complicated by Choroidal Neovascularization
Ophthalmic Genetics
Child Health
Ophthalmology
Pediatrics
Perinatology
Genetics
Bietti Crystalline Dystrophy
Identification of Novel CYP4V2 Genotypes Associated With Bietti Crystalline Dystrophy and Atypical Anterior Segment Phenotypes in Spanish Patients
Acta Ophthalmologica
Medicine
Ophthalmology
Current Perspectives in Bietti Crystalline Dystrophy
Clinical Ophthalmology
Ophthalmology
Genetic Testing for Bietti Crystalline Dystrophy
The EuroBiotech Journal
Characterization of Bietti Crystalline Dystrophy Patients withCYP4V2Mutations
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Clinical Course of Cone Dystrophy Caused by Mutations in the RPGR Gene
Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Clinical and Genetic Features in Italian Bietti Crystalline Dystrophy Patients
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
