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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2004-11-30
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pubmed:abstractText |
To identify the gene mutations in a pedigree with hereditary hemorrhagic telangiectasia.
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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 |
Sep
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pubmed:issn |
0253-2727
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pubmed:author |
pubmed-author:ChenPingP,
pubmed-author:DingQiu-lanQL,
pubmed-author:FuQi-huaQH,
pubmed-author:HuLi-mingLM,
pubmed-author:WangHong-liHL,
pubmed-author:WangWen-binWB,
pubmed-author:WangXue-fengXF,
pubmed-author:WuWen-manWM,
pubmed-author:XieBing-shouBS,
pubmed-author:XieShuangS,
pubmed-author:ZhengJia-yongJY,
pubmed-author:ZhouRong-fuRF,
pubmed-author:ZhuMiao-yongMY
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pubmed:issnType |
Print
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
536-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:15569532-Activin Receptors, Type II,
pubmed-meshheading:15569532-Aged,
pubmed-meshheading:15569532-Antigens, CD,
pubmed-meshheading:15569532-Base Sequence,
pubmed-meshheading:15569532-Codon, Nonsense,
pubmed-meshheading:15569532-DNA Mutational Analysis,
pubmed-meshheading:15569532-Exons,
pubmed-meshheading:15569532-Female,
pubmed-meshheading:15569532-Humans,
pubmed-meshheading:15569532-Male,
pubmed-meshheading:15569532-Pedigree,
pubmed-meshheading:15569532-Point Mutation,
pubmed-meshheading:15569532-Receptors, Cell Surface,
pubmed-meshheading:15569532-Telangiectasia, Hereditary Hemorrhagic
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pubmed:year |
2004
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pubmed:articleTitle |
[Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg479 Stop in the ALK-1 gene].
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pubmed:affiliation |
Wenzhou 3rd People's Hospital, Wenzhou 325000, China.
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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