Linked Life Data

12139570

Source:http://linkedlifedata.com/resource/pubmed/id/12139570

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2002-7-25
pubmed:abstractText
Gilbert's syndrome is a common inherited disorder of bilirubin metabolism contributing to the development of neonatal jaundice and causing recurrent jaundice after the neonatal period. In the patients with Gilbert's syndrome, mutations have been reported in the promoter and exons of the uridine diphosphate-glucuronosyl transferase 1 (UGT1A1) gene on chromsome 2q37, which encodes bilirubin uridine diphosphate-glucuronosyltransferase. However, the genetic basis of Gilbert's syndrome, including its inheritance trait, remains to be clarified.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1328-8067
pubmed:author
pubmed:issnType
Print
pubmed:volume
44
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
427-32
pubmed:dateRevised
2008-5-21
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.
pubmed:affiliation
Department of Development and Aging, Faculty of Medicine, Kobe University Graduate School of Medicine, Japan.
pubmed:publicationType
Journal Article