Linked Life Data

21231959

Source:http://linkedlifedata.com/resource/pubmed/id/21231959

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2011-4-7
pubmed:abstractText
To investigate the frequency of MEFV mutations and their associations with the clinical and laboratory findings in children with Henoch-Schönlein purpura (HSP).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1651-2227
pubmed:author
pubmed:copyrightInfo
© 2011 The Author(s)/Acta Paediatrica © 2011 Foundation Acta Paediatrica.
pubmed:issnType
Electronic
pubmed:volume
100
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
745-9
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Prevalence of MEFV gene mutations and their clinical correlations in Turkish children with Henoch-Schönlein purpura.
pubmed:affiliation
Department of Pediatric Nephrology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey.
pubmed:publicationType
Journal Article