Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy

INIS

• mutations 100%
• proteins 66%
• humans 50%
• phenotype 50%
• endothelium 50%
• cornea 50%
• antibodies 33%
• chromosomes 33%
• mice 16%
• data 16%
• genetics 16%
• interfaces 16%
• surfaces 16%
• interactions 16%
• genes 16%
• control 16%
• losses 16%
• usa 16%
• pathogenesis 16%
• membranes 16%
• mutants 16%
• messenger-rna 16%
• epithelium 16%
• exons 16%
• hearings 16%

Biochemistry, Genetics and Molecular Biology

• Mutation 83%
• Staining 66%
• Phenotype 50%
• Allele 33%
• Pedigree 33%
• Chromosome 16%
• Membrane 16%
• Nested Gene 16%
• Missense Mutation 16%
• Protein-Protein Interaction 16%
• Proband 16%
• Human 16%
• Computer Model 16%
• Autosomal Dominant Inheritance 16%
• Surface Property 16%
• Mouse 16%
• Dominant Inheritance 16%
• Chromosome 18q 16%
• Next Generation Sequencing 16%
• Mutant 16%
• Messenger RNA 16%
• Genetic Disorder 16%

Neuroscience

• Corneal Dystrophy 100%
• Phenotype 50%
• Cornea 50%
• Antibodies 33%
• Corneal Endothelium 33%
• Protein 33%
• Corneal Epithelium 16%
• Missense Mutation 16%
• Endothelium 16%
• Chromosome 16%
• Exon 16%
• Gene 16%
• Protein-Protein Interaction 16%
• Hearing Loss 16%