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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
1996-2-14
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pubmed:abstractText |
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.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0964-6906
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1625-8
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:8541850-Chromosome Mapping,
pubmed-meshheading:8541850-Chromosomes, Human, Pair 3,
pubmed-meshheading:8541850-Dementia,
pubmed-meshheading:8541850-Female,
pubmed-meshheading:8541850-Frontal Lobe,
pubmed-meshheading:8541850-Genetic Linkage,
pubmed-meshheading:8541850-Humans,
pubmed-meshheading:8541850-Male,
pubmed-meshheading:8541850-Pedigree
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pubmed:year |
1995
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pubmed:articleTitle |
Familial non-specific dementia maps to chromosome 3.
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pubmed:affiliation |
Department of Biochemistry and Molecular Genetics, St Mary's Hospital Medical School, London, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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