The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis
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 sea...
Main Authors: | , , , , |
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Format: | Article |
Language: | Portuguese |
Published: |
Elsevier
2013-09-01
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Series: | Jornal de Pediatria (Versão em Português) |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2255553613001006 |