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Influence of UGT1A1 Genetic Variants on Free Bilirubin Levels in Japanese Newborns

A Preliminary Study

Bibliographic Data

ID15469144
AuthorsHiroaki Hanafusa (0000-0002-6636-7724, Kobe University), Shinya Abe (0000-0002-9314-5617, Kobe University), Shohei Ohyama (0000-0003-3582-6390, Kobe University), Yuki Kyono (Kobe University), Takumi Kido (Kobe University), Ruka Nakasone (Kobe University), Mariko Ashina (Kobe University), Kenji Tanimura (0000-0003-1435-120X, Kobe University), Kandai Nozu (0000-0002-0290-3137, Kobe University), Kazumichi Fujioka (0000-0002-9913-6447, Kobe University, corresponding author)
Year2022
Volume19
Issue20
Pages13090-13090
Publication date2022-10-12
Open AccessYes
TypeARTICLE
VenueInternational Journal of Environmental Research and Public Health (JOURNAL)
Journal identifiersISSN: 1661-7827 • E-ISSN: 1660-4601
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/ijerph192013090
PMID36293671
OpenAlexW4304689323
LanguageEN
References cited42

This study is the first to show that the A allele in rs4148323 is a risk factor and that the (TA) 7 allele in rs3064744 is a protective factor for developing hyper-free bilirubinemia in Japanese newborns

Bilirubin · Biology · Hemoglobinopathies and Related Disorders · Medicine · Methemoglobinemia and Tumor Lysis Syndrome · Neonatal Health and Biochemistry · Genetics · Internal Medicine

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