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...
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Format: | Book |
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Brazilian Society of Pediatrics,
2013-09-01T00:00:00Z.
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A1234.567 |
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