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

Biochemistry, Genetics and Molecular Biology

• Allele 40%
• Antibody 40%
• Autosomal Dominant Inheritance 20%
• Chromosome 20%
• Chromosome 18q 20%
• Computer Model 20%
• Dominant Inheritance 20%
• Genetic Code 20%
• Genetic Disorder 20%
• Hearing 20%
• Human 20%
• Membrane 20%
• Messenger RNA 20%
• Missense Mutation 20%
• Mouse 20%
• Mutant 20%
• Mutation 100%
• Nested Gene 20%
• Next Generation Sequencing 20%
• Pedigree 40%
• Phenotype 60%
• Proband 20%
• Protein 40%
• Protein-Protein Interaction 20%
• Staining 80%
• Surface Property 20%

INIS

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

Neuroscience

• Antibodies 33%
• Chromosome 16%
• Cornea 50%
• Corneal Dystrophy 100%
• Corneal Endothelium 33%
• Corneal Epithelium 16%
• Endothelium 16%
• Exon 16%
• Gene 16%
• Hearing Loss 16%
• Missense Mutation 16%
• Phenotype 50%
• Protein 33%
• Protein-Protein Interaction 16%
• Staining Technique 66%