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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1985-11-13
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
|
| pubmed:issn |
0022-3476
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
107
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
564-6
|
| pubmed:dateRevised |
2005-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:4045606-Alleles,
pubmed-meshheading:4045606-Complement C3,
pubmed-meshheading:4045606-Complement C3b,
pubmed-meshheading:4045606-Female,
pubmed-meshheading:4045606-Hemolytic-Uremic Syndrome,
pubmed-meshheading:4045606-Humans,
pubmed-meshheading:4045606-Infant,
pubmed-meshheading:4045606-Recurrence
|
| pubmed:year |
1985
|
| pubmed:articleTitle |
Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|