| pubmed-article:15387979 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0152035 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0228174 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0270612 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0815275 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0852949 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0021308 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C1417768 | lld:lifeskim |
| pubmed-article:15387979 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:15387979 | pubmed:issue | 14 | lld:pubmed |
| pubmed-article:15387979 | pubmed:dateCreated | 2004-9-24 | lld:pubmed |
| pubmed-article:15387979 | pubmed:abstractText | To search for mutations in NOTCH3 gene in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). | lld:pubmed |
| pubmed-article:15387979 | pubmed:language | chi | lld:pubmed |
| pubmed-article:15387979 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15387979 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15387979 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15387979 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15387979 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15387979 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15387979 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15387979 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:15387979 | pubmed:issn | 0376-2491 | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:ZhangZhuoZ | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:ZhangYingY | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:LuHeH | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:YuanYunY | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:BuDing-fangDF | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:HuangYi-ningY... | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:WangZhao-xiaZ... | lld:pubmed |
| pubmed-article:15387979 | pubmed:author | pubmed-author:NiuXiao-yuanX... | lld:pubmed |
| pubmed-article:15387979 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15387979 | pubmed:day | 17 | lld:pubmed |
| pubmed-article:15387979 | pubmed:volume | 84 | lld:pubmed |
| pubmed-article:15387979 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15387979 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15387979 | pubmed:pagination | 1175-80 | lld:pubmed |
| pubmed-article:15387979 | pubmed:dateRevised | 2010-3-23 | lld:pubmed |
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| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:meshHeading | pubmed-meshheading:15387979... | lld:pubmed |
| pubmed-article:15387979 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15387979 | pubmed:articleTitle | [NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]. | lld:pubmed |
| pubmed-article:15387979 | pubmed:affiliation | Department of Neurology, Peking University First Hospital, Beijing 100034, China. | lld:pubmed |
| pubmed-article:15387979 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15387979 | pubmed:publicationType | English Abstract | lld:pubmed |
