Autosomal dominant frontotemporal lobar degeneration: From genotype to phenotype

Medicine & Life Sciences

• Frontotemporal Lobar Degeneration 100%
• Frontotemporal Dementia 66%
• Genotype 50%
• Phenotype 42%
• Microtubule-Associated Proteins 42%
• Mutation 29%
• Progranulins 27%
• Modifier Genes 25%
• Chromosomes, Human, Pair 9 23%
• Motor Neuron Disease 22%
• Aphasia 20%
• Open Reading Frames 17%
• High-Throughput Nucleotide Sequencing 17%
• Age of Onset 16%
• Genes 14%
• Alzheimer Disease 13%
• Population 6%
• Proteins 6%

Chemical Compounds

• Mutation 60%
• Protein 29%
• Heterogeneity 21%