Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations.

Medicine and Dentistry

• Frontotemporal Lobar Degeneration 100%
• Aphasia 100%
• Tau 50%
• Clinical Feature 50%
• Genetic Screening 50%
• Gene Mutation 50%
• Compulsive Behavior 50%
• TDP 43 Proteinopathy 50%
• Stereotypy 50%
• Dietary Change 50%
• Symptom 50%

Neuroscience

• Aphasia 100%
• Frontotemporal Dementia 100%
• Behavior (Neuroscience) 50%
• Disinhibition 50%
• Compulsive Behavior 50%
• Gene Mutation 50%
• Stereotypy 50%

Biochemistry, Genetics and Molecular Biology

• C9orf72 100%
• Genotyping 12%
• Transactive Response Dna Binding Protein-43 12%
• Tau 12%
• Genetic Screening 12%
• Gene Mutation 12%
• Stereotypy 12%