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...
Saved in:
Main Authors: | Jiebo Liu (Author), Jun Long (Author), Shaofang Zhang (Author), Xiaoyan Fang (Author), Yuyuan Luo (Author) |
---|---|
Format: | Book |
Published: |
Brazilian Society of Pediatrics,
2013-09-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis
by: Jiebo Liu, et al.
Published: (2013) -
Impacto dos polimorfismos genéticos SLCO1B1 sobre a hiperbilirrubinemia neonatal: revisão sistemática com metanálise
by: Jiebo Liu, et al.
Published: (2013) -
Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population
by: Chalirmporn Atasilp, et al.
Published: (2022) -
Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population
by: Juan Fan, et al.
Published: (2024) -
SLCO1B1 c.388A > G variant incidence and the severity of hyperbilirubinemia in Indonesian neonates
by: Radhian Amandito, et al.
Published: (2019)