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15030995
Source:
http://linkedlifedata.com/resource/pubmed/id/15030995
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53
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0011155
,
umls-concept:C0017337
,
umls-concept:C0109547
,
umls-concept:C0205225
,
umls-concept:C0314603
,
umls-concept:C0332120
,
umls-concept:C0936012
,
umls-concept:C1412328
,
umls-concept:C1457869
pubmed:issue
4
pubmed:dateCreated
2004-3-19
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8503886
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Bile Acids and Salts
,
http://linkedlifedata.com/resource/pubmed/chemical/DNA
,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases
,
http://linkedlifedata.com/resource/pubmed/chemical/cholestenone 5 beta-reductase
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0168-8278
pubmed:author
pubmed-author:BaussanChristianeC
,
pubmed-author:CresteilDanièleD
,
pubmed-author:DabadieAlainA
,
pubmed-author:GerhardtMarie-FrançoiseMF
,
pubmed-author:GonzalesEmmanuelE
,
pubmed-author:JacqueminEmmanuelE
pubmed:issnType
Print
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
716-8
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15030995-Base Sequence
,
pubmed-meshheading:15030995-Bile Acids and Salts
,
pubmed-meshheading:15030995-DNA
,
pubmed-meshheading:15030995-DNA Mutational Analysis
,
pubmed-meshheading:15030995-Diseases in Twins
,
pubmed-meshheading:15030995-Exons
,
pubmed-meshheading:15030995-Female
,
pubmed-meshheading:15030995-Heterozygote
,
pubmed-meshheading:15030995-Humans
,
pubmed-meshheading:15030995-Infant
,
pubmed-meshheading:15030995-Liver Failure
,
pubmed-meshheading:15030995-Metabolism, Inborn Errors
,
pubmed-meshheading:15030995-Oxidoreductases
,
pubmed-meshheading:15030995-Point Mutation
,
pubmed-meshheading:15030995-Twins, Monozygotic
pubmed:year
2004
pubmed:articleTitle
SRD5B1 (AKR1D1) gene analysis in delta(4)-3-oxosteroid 5beta-reductase deficiency: evidence for primary genetic defect.
pubmed:publicationType
Letter
,
Case Reports