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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
14
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pubmed:dateCreated |
2004-9-24
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pubmed:abstractText |
To search for mutations in NOTCH3 gene in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
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pubmed:language |
chi
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0376-2491
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
17
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pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1175-80
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pubmed:dateRevised |
2010-3-23
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pubmed:meshHeading |
pubmed-meshheading:15387979-Adult,
pubmed-meshheading:15387979-Aged,
pubmed-meshheading:15387979-Base Sequence,
pubmed-meshheading:15387979-Cerebral Infarction,
pubmed-meshheading:15387979-DNA Mutational Analysis,
pubmed-meshheading:15387979-Dementia, Multi-Infarct,
pubmed-meshheading:15387979-Exons,
pubmed-meshheading:15387979-Female,
pubmed-meshheading:15387979-Genes, Dominant,
pubmed-meshheading:15387979-Heterozygote,
pubmed-meshheading:15387979-Humans,
pubmed-meshheading:15387979-Male,
pubmed-meshheading:15387979-Middle Aged,
pubmed-meshheading:15387979-Molecular Sequence Data,
pubmed-meshheading:15387979-Mutation, Missense,
pubmed-meshheading:15387979-Pedigree,
pubmed-meshheading:15387979-Point Mutation,
pubmed-meshheading:15387979-Proto-Oncogene Proteins,
pubmed-meshheading:15387979-Receptors, Cell Surface,
pubmed-meshheading:15387979-Receptors, Notch
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pubmed:year |
2004
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pubmed:articleTitle |
[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
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pubmed:affiliation |
Department of Neurology, Peking University First Hospital, Beijing 100034, China.
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pubmed:publicationType |
Journal Article,
English Abstract
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