Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1

Medicine and Dentistry

• Rod-Cone Dystrophy 100%
• Family 80%
• Diseases 60%
• Retina Dystrophy 60%
• Exon 20%
• Phenotype 20%
• Prevalence 20%
• Protein 20%
• Messenger RNA 20%
• Null Allele 20%
• Onset Age 20%
• Chromosome 15 20%
• Retinitis 20%
• Retinoid Binding Protein 20%
• Gene 20%
• Arm 20%
• Marker 20%
• Clotiazepam 20%
• Gene Linkage 20%

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• Nested Gene 20%
• Binding Protein 20%
• Phenotype 20%
• Null Allele 20%
• Prevalence 20%
• Gene Mutation 20%
• Age 20%
• Contrast 20%
• Protein 20%
• Chromosome 15 20%