Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Relationship between glucose-6-phosphate dehydrogenase gene mutations and neonatal jaundice in Naning, Guangxi].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Dec 2009

Zhong Dan-Ni, Gao Zong-Yan, Liu You-Nan, Liu Yi, Wei Lu-Ming

Abstract excerpt

OBJECTIVE: To study the correlation between glucose-6-phosphate dehydrogenase (G-6-PD) activities and three common mutations of G-6-PD gene G1388A, G1376T and A95G and investigate the effects of G-6-PD gene mutations on neonatal jaundice in Nanning, Guangxi. METHODS: One hundred and twenty-four n...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bilirubin
Share to Encephalitis
Share to Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Infant, Newborn

Share to Jaundice, Neonatal

Share to Prohibitins

Source

Identifiers

PMID: 20113600

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20113600-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Relationship between glucose-6-phosphate dehydrogenase gene mutations and neonatal jaundice in Naning, Guangxi].PMID 20113600Read ↗

[Role of genetic factors in occurrence of neonatal jaundice in Guangxi region].Semantic proximity Read ↗

[Correlation analysis of genotypes and the enzymatic activities of glucose-6-phosphate dehydrogenase in neonates in Guangzhou].Semantic proximity Read ↗

[Genetic Mutation Characteristics of Glucose-6-Phosphate Dehydrogenase Deficiency Patients in Wuhan].Semantic proximity Read ↗

Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infantsSemantic proximity Read ↗

Co-Inheritance of G6PD Deficiency and 211 G to A Variation of UGT1A1 in Neonates with Hyperbilirubinemia In Eastern GuangdongSemantic proximity Read ↗

[Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].Semantic proximity Read ↗

[Molecular characterization of glucose-6-phosphate dehydrogenase variants in four ethnic groups in Yunnan province of China].Semantic proximity Read ↗

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

Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian.Semantic proximity Read ↗

Three mutations analysis of glucose-6-phosphate dehydrogenase deficiency in neonates in South-west China.Semantic proximity Read ↗

[Screening results and genetic features of glucose-6-phosphate dehydrogenase deficiency in 54 025 preterm infants in Chengdu, China].Semantic proximity Read ↗

Investigation of the Association Between G6PD, UGT1A1, and SLCO1B1 Gene Polymorphisms and Neonatal Hyperbilirubinemia Using MALDI-TOF MS TechnologySemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.