pubmed-article:18254984 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18254984 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
pubmed-article:18254984 | lifeskim:mentions | umls-concept:C0009447 | lld:lifeskim |
pubmed-article:18254984 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
pubmed-article:18254984 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
pubmed-article:18254984 | lifeskim:mentions | umls-concept:C1332838 | lld:lifeskim |
pubmed-article:18254984 | lifeskim:mentions | umls-concept:C0240795 | lld:lifeskim |
pubmed-article:18254984 | pubmed:dateCreated | 2008-3-27 | lld:pubmed |
pubmed-article:18254984 | pubmed:abstractText | Common variable immunodeficiency (CVID) comprises a heterogeneous group of primary antibody deficiencies with complex clinical and immunological phenotypes. The recent discovery that some CVID patients show monogenic defects in the genes encoding ICOS, TACI or CD19 prompted us to investigate several functional candidate genes in individuals with CVID. | lld:pubmed |
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pubmed-article:18254984 | pubmed:language | eng | lld:pubmed |
pubmed-article:18254984 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18254984 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:18254984 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18254984 | pubmed:issn | 1471-2172 | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:PlebaniAlessa... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:HUBERH PHP | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:SchäfferAleja... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:HammarströmLe... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:MoscheseVivia... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:LougarisVassi... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:GrimbacherBod... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:Pan-Hammarstr... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:MetinAyseA | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:ThielJensJ | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:WebsterDavid... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:DuLikunL | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:JungJohannesJ | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:WoellnerCrist... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:BirmelinJenni... | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:NeumannCarlaC | lld:pubmed |
pubmed-article:18254984 | pubmed:author | pubmed-author:HagenaTinaT | lld:pubmed |
pubmed-article:18254984 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18254984 | pubmed:volume | 9 | lld:pubmed |
pubmed-article:18254984 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18254984 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18254984 | pubmed:pagination | 3 | lld:pubmed |
pubmed-article:18254984 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
pubmed-article:18254984 | pubmed:meshHeading | pubmed-meshheading:18254984... | lld:pubmed |
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pubmed-article:18254984 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18254984 | pubmed:articleTitle | Screening of functional and positional candidate genes in families with common variable immunodeficiency. | lld:pubmed |