Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to n...
Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population
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Author / Creator
Fan, Juan , He, Hua-Yun , Li, Huan-Huan , Wu, Pi-Liu , Tang, Lei , Deng, Bo-Yin , Dong, Wen-Hui and Wang, Jian-Hui
Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
Severe neonatal hyperbilirubinemia could lead to kernicterus and neonatal death. This study aimed to analyze the association between single nucleotide polymorphisms in genes involved in bilirubin metabolism and the incidence of severe hyperbilirubinemia.
A total of 144 neonates with severe hyperbilirubinemia and 50 neonates without or mild hyper...
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Full title
Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_8959b01a7dff4f489f0e98bca02b3399
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_8959b01a7dff4f489f0e98bca02b3399
Other Identifiers
ISSN
1471-2431
E-ISSN
1471-2431
DOI
10.1186/s12887-024-04537-0