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PMID: 8541850 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Familial non-specific dementia maps to chromosome 3.

Human molecular genetics ·Vol. 4 ·No. 9 ·1995-09-00 ·Pages 1625-8

Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy J, Collinge J

Abstract

A significant minority of degenerative dementias lack distinctive inclusion bodies, plagues or tangles on pathological examination. Half of these cases have a positive family history of dementia. We have studied the largest published family with such a dementia and mapped the disease locus to a 12 cM region of chromosome 3 spanning the centromere. Haplotype analysis demonstrates a common region shared between all affected individuals between the markers D3S1284 and D3S1603. Like a number of other late onset neurodegenerative diseases, the disease presents at an earlier age when paternally inherited.

MeSH Terms
Chromosome Mapping Chromosomes, Human, Pair 3 Dementia/genetics Female Frontal Lobe/pathology Genetic Linkage Humans Male Pedigree
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Brown J
Department of Biochemistry and Molecular Genetics, St Mary's Hospital Medical School, London, UK.
Ashworth A
Gydesen S
Sorensen A
Rossor M
Hardy J
Collinge J
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
Published
1995-09-00
Pages
1625-8
Language
English
Region
England
NLM ID
9208958
Subset
IM
Grants
Wellcome Trust · United Kingdom
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