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RDH12
Genetic Analysis of Retinopathy in Type 1 Diabetes
Expanding the Phenotypic Spectrum in RDH12-Associated Retinal Disease
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Examination of Testicular Gene Expression Patterns in Yorkshire Pigs with High and Low Levels of Boar Taint
Comparative Analysis of the Domestic Cat Genome Reveals Genetic Signatures Underlying Feline Biology and Domestication
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
RDH12 Mutations Cause a Severe Retinal Degeneration with Relatively Spared Rod Function
Comprehensive Genotyping Reveals RPE65 As the Most Frequently Mutated Gene in Leber Congenital Amaurosis in Denmark
Involvement of Oxidative and Endoplasmic Reticulum Stress in RDH12-Related Retinopathies
Determining the Causes of Recessive Retinal Dystrophy
Development of Gene Therapy for the Treatment of Retinal Dystrophies Caused by Mutations in AIPL1
Chromosome 14 Deletions, Rings, and Epilepsy Genes: a Riddle Wrapped in a Mystery Inside an Enigma
ABSTRACT Using a Bioinformatics Approach to Identify Genes That
EPSTEIN BARR VIRUS ENCODED Microrna from the BHRF1- CLUSTER IS INVOLVED in VIRAL SUPPRESSION DURING LATENCY
Association of a Novel Mutation in the Retinol Dehydrogenase 12 (RDH12) Gene with Autosomal Dominant Retinitis Pigmentosa
Molecular Genetics of Infantile-Onset Retinal Dystrophies
Whole-Exome Sequencing Identifies Two Novel ALMS1 Mutations in Indian Patients with Leber Congenital Amaurosis
Current Concepts of Genotype-Phenotype Correlations
Top View
Graded Gene Expression Changes Determine Phenotype Severity in Mouse Models of CRX-Associated Retinopathies Philip A
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Mutations in RDH12 Encoding a Photoreceptor Cell Retinol Dehydrogenase Cause Childhood-Onset Severe Retinal Dystrophy
Leber Congenital Amaurosis and Other Autosomal
Retinal Gene Distribution and Functionality Implicated in Inherited Retinal Degenerations Can Reveal Disease-Relevant Pathways for Pharmacologic Intervention
Genetic Screening of LCA in Belgium: Predominance of CEP290 and Identification of Potential Modifier Alleles in AHI1 of CEP290-R
Genetic Network Regulating Visual Acuity Makes Limited Contribution
Global Analysis of Protein Expression of Inner Ear Hair Cells
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