A large calabrian kindred segregating frontotemporal dementia

Frontotemporal dementia (FTD) displays significant neuropathological and genetic heterogeneity among and within affected families. An early diagnosis is often difficult because cognitive symptoms are manifest only at a late stage of the disease. We have been studying a large pedigree segregating fro...

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Veröffentlicht in:	Journal of neurology 2002-07, Vol.249 (7), p.911-922
Hauptverfasser:	CURCIO, S. A. M, KAWARAI, T, BRUNI, A. C, PATERSON, A. D, MALETTA, R. G, PUCCIO, G, PERRI, M, DI NATALE, M, PALERMO, S, FONCIN, J.-F, HYSLOP, P. H. St. George
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Aged Alzheimer's disease Biological and medical sciences Chromosome Mapping Chromosomes Chromosomes, Human, Pair 17 - genetics Chromosomes, Human, Pair 3 - genetics Chromosomes, Human, Pair 9 - genetics Dementia Dementia - genetics Female Genealogy and Heraldry Humans Italy Male Medical sciences Memory Middle Aged Mutation Neurology Neuropsychology Pedigree
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