Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese-Reference-Cited by-同舟云学术

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Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese

Published:1999-01 Issue:1 Volume:44 Page:22-25
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Akaba Kazuhiro,Kimura Toshiyuki,Sasaki Ayako,Tanabe Saori,Wakabayashi Takashi,Hiroi Masahiko,Yasumura Seiji,Maki Kazuko,Aikawa Shogo,Hayasaka K.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg19995.pdf

Cited by 71 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan;ESMO Open;2023-02

3. Influence of UGT1A1 Genetic Variants on Free Bilirubin Levels in Japanese Newborns: A Preliminary Study;International Journal of Environmental Research and Public Health;2022-10-12

4. Contribution of genetic factors to high rates of neonatal hyperbilirubinaemia on the Thailand-Myanmar border;PLOS Global Public Health;2022-06-17

5. Genotypic and phenotypic landscapes of 51 pharmacogenes derived from whole-genome sequencing in a Thai population;PLOS ONE;2022-02-17

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