NR ABTM

AU Brown,J.; Smith,S.; Brun,A.; Collinge,J.; Gydesen,S.; Hardy,J.; Mullan,M.; Goate,A.

TI Genetic characterization of a novel familial dementia

QU Annals of the New York Academy of Sciences 1991; 640: 181-3

PT journal article

AB Clinical and neuropathologic findings from a Danish family in which a dementing illness is segregating as an apparent autosomal dominant disorder were previously described (Gydesen et al. 1987). We present here genetic findings from this family in which linkage analysis has excluded Huntington's disease and chromosome 21-encoded Alzheimer's disease. None of the known prion mutations has been detected in affected individuals from this family. However, linkage analysis with the prion gene has been uninformative. This family probably represents a novel genetic dementia.

MH DNA Probes; Dementia/*genetics; *Gene Amplification; Human; Pedigree; Polymerase Chain Reaction

AD Department of Biochemistry, St. Mary's Hospital Medical School, London, United Kingdom.

SP englisch

PO USA

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