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18400199
Source:
http://linkedlifedata.com/resource/pubmed/id/18400199
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pubmed-article:18400199
rdf:type
pubmed:Citation
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pubmed-article:18400199
lifeskim:mentions
umls-concept:C0042909
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pubmed-article:18400199
pubmed:issue
6
lld:pubmed
pubmed-article:18400199
pubmed:dateCreated
2008-5-27
lld:pubmed
pubmed-article:18400199
pubmed:abstractText
To investigate whether the LOC387715 polymorphism is associated with polypoidal choroidal vasculopathy (PCV) and with vitreous hemorrhage (VH), one of the most severe clinical phenotypes, in the Japanese population.
lld:pubmed
pubmed-article:18400199
pubmed:language
eng
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pubmed-article:18400199
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pubmed:citationSubset
AIM
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pubmed:status
MEDLINE
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pubmed-article:18400199
pubmed:month
Jun
lld:pubmed
pubmed-article:18400199
pubmed:issn
0002-9394
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pubmed-article:18400199
pubmed:author
pubmed-author:ImasawaMitsuh...
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pubmed-article:18400199
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pubmed-author:IijimaHiroyuk...
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pubmed-author:KubotaTakeoT
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pubmed:author
pubmed-author:TanabeNaohiko...
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pubmed:issnType
Print
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pubmed:volume
145
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pubmed:owner
NLM
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pubmed-article:18400199
pubmed:authorsComplete
Y
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pubmed:pagination
1058-1062
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pubmed-article:18400199
pubmed:year
2008
lld:pubmed
pubmed-article:18400199
pubmed:articleTitle
Association of LOC387715 A69S with vitreous hemorrhage in polypoidal choroidal vasculopathy.
lld:pubmed
pubmed-article:18400199
pubmed:affiliation
Department of Ophthalmology, Faculty of Medicine, University of Yamanashi, Shimokato 1110, Chuo City, Yamanashi, Japan.
lld:pubmed
pubmed-article:18400199
pubmed:publicationType
Journal Article
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entrez-gene:387715
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