Underestimation of the contribution of 211 G to A variation in UGT1A1 to neonatal hyperbilirubinemia in China

Mei, et al assessed genetic variation present in a cohort of 1412 neonates with unconjugated hyperbilirubinemia in China.1 A genetic variant was observed in 55 participants (4%); 45 had variants in genes associated with unconjugated hyperbilirubinemia, including 18% with variants in UGT1A1.

source https://www.jpeds.com/article/S0022-3476(22)00284-0/fulltext?rss=yes

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