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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1997-6-25
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0340-6199
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
156
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
247-8
|
| pubmed:dateRevised |
2010-11-18
|
| pubmed:meshHeading |
pubmed-meshheading:9083771-Child,
pubmed-meshheading:9083771-Clusterin,
pubmed-meshheading:9083771-Congenital Disorders of Glycosylation,
pubmed-meshheading:9083771-Diagnosis, Differential,
pubmed-meshheading:9083771-Glycoproteins,
pubmed-meshheading:9083771-Humans,
pubmed-meshheading:9083771-Molecular Chaperones
|
| pubmed:year |
1997
|
| pubmed:articleTitle |
Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG)
|
| pubmed:publicationType |
Letter
|