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Article

Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.

BMC pediatrics - 11 Dec 2021

Xu Jia-Xin, Lin Fen, Chen Zi-Kai, Luo Zhao-Yun, Zhan Xiao-Fen, Wu Jiao-Ren, Ma Yu-Bin, Li Jian-Dong, Yang Li-Ye

Abstract excerpt

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which may manifest as neonatal hyperbilirubinemia, is the most prevalent erythrocytic enzyme-related disease in the world. OBJECTIVE: To investigate the association between neonatal hyperbilirubinemia and co-inheritance of G6PD deficiency and 211 G to A variation of UGT1A1 in Chaozhou city of eastern Guangdong province, the effects of G6PD...

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Identifiers

PMID: 34895177
DOI: 10.1186/s12887-021-03010-6
PMCID: PMC8665559

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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