Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family

• Rademakers, R.
• Broeck, M. van den
• Sleegers, K.
• Duijn, C.M. van
• Broeckhoven, C. van
• Cruts, M.

February 2004
Letter To Editor

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• Human
• Support, Non-U.S. Gov't
• Aged
• Middle Aged
• Membrane Proteins/*genetics
• tau Proteins/*genetics
• 0 (Membrane Proteins)
• Dementia/*genetics/*pathology
• 0 (Microtubule-Associated Proteins)
• Frontal lobe dementia
• 0 (tau Proteins)
• 0 (presenilin-2)
• 0 (FTDP-17 protein)
• Microtubule-Associated Proteins/*genetics

• mutation
• psh 2
• dementia
• family
• mutation analysis
• presenilin
• analysis
• van duijn c
• van broeckhoven m
• tau-negative
• presenilin homologue 2
• novel
• frontotemporal dementia
• 17 q 21.
• 17 q 21
• research
• patient
• linkage
• homologue
• haplotype