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19012342
Source:
http://linkedlifedata.com/resource/pubmed/id/19012342
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41
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0012634
,
umls-concept:C0013720
,
umls-concept:C0026882
,
umls-concept:C0030705
,
umls-concept:C0332197
,
umls-concept:C0549185
,
umls-concept:C0678227
,
umls-concept:C1423007
pubmed:issue
24
pubmed:dateCreated
2008-12-1
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Collagen Type V
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1552-4833
pubmed:author
pubmed-author:ColeWilliam GWG
,
pubmed-author:DodsonGerald EGE
,
pubmed-author:GreenspanDaniel SDS
,
pubmed-author:HoffmanGuy GGG
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
146A
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3240-1
pubmed:meshHeading
pubmed-meshheading:19012342-Alleles
,
pubmed-meshheading:19012342-Collagen Diseases
,
pubmed-meshheading:19012342-Collagen Type V
,
pubmed-meshheading:19012342-DNA Mutational Analysis
,
pubmed-meshheading:19012342-Ehlers-Danlos Syndrome
,
pubmed-meshheading:19012342-Female
,
pubmed-meshheading:19012342-Humans
,
pubmed-meshheading:19012342-Male
,
pubmed-meshheading:19012342-Mutation
pubmed:year
2008
pubmed:articleTitle
Absence of apparent disease causing mutations in COL5A3 in 13 patients with hypermobility Ehlers-Danlos syndrome.
pubmed:affiliation
Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, Wisconsin 53706, USA.
pubmed:publicationType
Journal Article