Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease

Keyphrases

• Clinical Phenotype 100%
• Presenilin 1 mutation 100%
• Familial Alzheimer's Disease 100%
• Seizure 40%
• Presenilin 40%
• Cognitive Decline 20%
• Autosomal Dominant 20%
• Phosphorylated tau 20%
• Guanine 20%
• Frontal Cortex 20%
• Pathological Findings 20%
• Codon 20%
• Single nucleotide Variant 20%
• Genetic mutation 20%
• Histopathological Examination 20%
• Amyloid Deposition 20%
• Exon 7 20%
• Confirmed Cases 20%
• Rapid Deterioration 20%
• Amyloid Protein Precursor 20%
• Rapidly Progressive 20%
• Presenilin 2 20%
• Early-onset AD 20%
• Penetrance 20%
• Tau Deposition 20%

Neuroscience

• Presenilin 1 100%
• Familial Alzheimer's Disease 100%
• Frontal Lobe 20%
• Codon 20%
• Exon 20%
• Gene Mutation 20%
• Amyloid Precursor Protein 20%
• Adenine 20%
• Guanine 20%
• Presenilin 2 20%
• Amyloid Protein 20%