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Publications by Luminita Moruz
Homozygosity Mapping in Patients With Cone–Rod Dystrophy: Novel Mutations and Clinical Characterizations
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Recognizing Uncertainty Increases Robustness and Reproducibility of Mass Spectrometry-Based Protein Inferences
Journal of Proteome Research
Biochemistry
Chemistry
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Novel CDHR1 Mutation Causing Cone Rod Dystrophy
Acta Ophthalmologica
Medicine
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Novel C8ORF37 Mutation Causing Cone Rod Dystrophy
Acta Ophthalmologica
Medicine
Ophthalmology
Cone Dystrophy With Supernormal Rod Response Is Strictly Associated With Mutations inKCNV2
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome
Rod-Cone Dystrophy in Spinocerebellar Ataxia Type 1
Archives of Ophthalmology
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
Cone-Rod Dystrophy and Amelogenesis Imperfecta (Jalili Syndrome): Phenotypes and Environs
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Mild Cone‐rod Dystrophy and Sensorineural Hearing Loss With CEP250 Mutation in a Japanese Family
Acta Ophthalmologica
Medicine
Ophthalmology