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| pubmed-article:10632659 | pubmed:dateCreated | 2000-3-2 | lld:pubmed |
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| pubmed-article:10632659 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:10632659 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:10632659 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10632659 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:10632659 | pubmed:issn | 0009-9104 | lld:pubmed |
| pubmed-article:10632659 | pubmed:author | pubmed-author:OrrenAA | lld:pubmed |
| pubmed-article:10632659 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10632659 | pubmed:volume | 119 | lld:pubmed |
| pubmed-article:10632659 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10632659 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10632659 | pubmed:pagination | 255-8 | lld:pubmed |
| pubmed-article:10632659 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:10632659 | pubmed:meshHeading | pubmed-meshheading:10632659... | lld:pubmed |
| pubmed-article:10632659 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:10632659 | pubmed:articleTitle | Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects. | lld:pubmed |
| pubmed-article:10632659 | pubmed:publicationType | Editorial | lld:pubmed |
| pubmed-article:10632659 | pubmed:publicationType | Review | lld:pubmed |
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