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

[Gene Mutants and Their Clinical Characteristics of G6PD Deficiency Among Children in Luzhou Area].

Zhongguo shi yan xue ye xue za zhi - 1 Jun 2020

Jiang Qi, Deng Zheng-Hua, Chen Hong-Ying, Yang Hong, Liu Wen-Jun

Abstract excerpt

OBJECTIVE: To study the gene mutants of G6PD deficiency and their clinical featuers among children in Luzhou area. METHODS: 732 children with suspected G6PD deficiency in Luzhou area from March 2017 to July 2019 were selected, which were examined for G6PD enzyme activity and gene mutation. The G6PD enzyme activity was detected by ultraviolet rate quantification, and the gene mutation was detected by melting curve...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Glucosephosphate Dehydrogenase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Hemolysis

Share to Mutation

Source

Identifiers

PMID: 32552971
DOI: 10.19746/j.cnki.issn.1009-2137.2020.03.046

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

[Gene Mutants and Their Clinical Characteristics of G6PD Deficiency Among Children in Luzhou Area].PMID 32552971Read ↗

Screening results and mutation frequency analysis of G6PD deficiency in 1,291,274 newborns in Huizhou, China: a twenty-year experience.Semantic proximity Read ↗

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017Semantic proximity Read ↗

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

The gene spectrum of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Guangdong province, China.Semantic proximity Read ↗

[Molecular epidemiology of G6PD deficiency in Chaozhou area of eastern Guangdong Province].Semantic proximity Read ↗

[Identification of G6PD gene mutations in several nationalities from Yunnan province].Semantic proximity Read ↗

[G6PD gene mutations in Guangxi, China].Semantic proximity Read ↗

[Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Han and Li nationalities in Hainan, China and identification of a new mutation in human G6PD gene].Semantic proximity Read ↗

[Glucose-6-phosphate dehydrogenase gene mutations in She nationality, Fujian province].Semantic proximity Read ↗

[G6PD Gene Mutations in Shui people in Sandu of Guizhou].Semantic proximity Read ↗

[Identification of G6PD gene variants from Hakka population in Guangdong province].Semantic proximity Read ↗

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