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Article

The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis.

Jornal de pediatria - 1 Jan 2000

Liu Jiebo, Long Jun, Zhang Shaofang, Fang Xiaoyan, Luo Yuyuan

Abstract excerpt

OBJECTIVE: To determine whether three variants (388 G>A, 521 T>C, and 463 C>A) of the solute carrier organic anion transporter family member 1B1 (SLCO1B1) are associated with neonatal hyperbilirubinemia. DATA SOURCE: The China National Knowledge Infrastructure and MEDLINE databases were searched. The systematic review with meta-analysis included genetic studies which assessed the association between neonatal...

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PMID: 23850112
DOI: 10.1016/j.jped.2013.01.008

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The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis.PMID 23850112Read ↗

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UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?Semantic proximity Read ↗

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