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rdf:type |
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|
lifeskim:mentions |
|
|
pubmed:issue |
5
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pubmed:dateCreated |
2005-4-18
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|
pubmed:abstractText |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is caused by mutations of the Notch3 gene on 19p13. Varying phenotypic expression leads to under recognition and misdiagnosis. Prevalence therefore remains uncertain. We sought to estimate the prevalence of CADASIL in the west of Scotland.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0022-3050
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
76
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pubmed:owner |
NLM
|
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pubmed:authorsComplete |
Y
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pubmed:pagination |
739-41
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pubmed:dateRevised |
2008-11-20
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pubmed:meshHeading |
pubmed-meshheading:15834040-Adolescent,
pubmed-meshheading:15834040-Adult,
pubmed-meshheading:15834040-CADASIL,
pubmed-meshheading:15834040-Catchment Area (Health),
pubmed-meshheading:15834040-Chromosomes, Human, Pair 19,
pubmed-meshheading:15834040-Female,
pubmed-meshheading:15834040-Humans,
pubmed-meshheading:15834040-Male,
pubmed-meshheading:15834040-Phenotype,
pubmed-meshheading:15834040-Point Mutation,
pubmed-meshheading:15834040-Polymerase Chain Reaction,
pubmed-meshheading:15834040-Prevalence,
pubmed-meshheading:15834040-Proto-Oncogene Proteins,
pubmed-meshheading:15834040-Receptors, Cell Surface,
pubmed-meshheading:15834040-Receptors, Notch,
pubmed-meshheading:15834040-Registries,
pubmed-meshheading:15834040-Scotland
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|
pubmed:year |
2005
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|
pubmed:articleTitle |
The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland.
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|
pubmed:affiliation |
Division of Clinical Neurosciences, Institute of Neurological Sciences, Southern General Hospital, 1345 Govan Road, Glasgow G3 8QB, Scotland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
