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

Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system.

Human heredity - 1 Jun 1999

Du C S, Ren X, Chen L, Jiang W, He Y, Yang M

Abstract excerpt

Glucose-6-phosphate dehydrogenase (G6PD) is the most common human enzymopathy. To date more than 122 mutations in the G6PD gene have been discovered, among which 12 point mutations are found in the Chinese. The 2 most common mutations, G1388A and G1376T, account for more than 50% of mutations rep...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to China
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Genetic Testing

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Point Mutation

Source

Identifiers

PMID: 10364676
DOI: 10.1159/000022860

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10364676-2026-09-02.2. 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

Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system.PMID 10364676Read ↗

[Detection of three common G6PD gene point mutations in Guangdong province by using ARMS].Semantic proximity Read ↗

Reduction of Missed Diagnosis of G6PD Deficiency in Heterozygous Females by G6PD/6PGD Ratio Assay Combined with Amplification Refractory Mutation System PCR.Semantic proximity Read ↗

STARD-rapid screening for the 6 most common G6PD gene mutations in the Chinese population using the amplification refractory mutation system combined with melting curve analysis.Semantic proximity Read ↗

Denaturing high-performance liquid chromatography technique platform applied to screen G6PD deficient variants.Semantic proximity Read ↗

Rapid detection of six common Chinese G6PD mutations by MALDI-TOF MS.Semantic proximity Read ↗

Identification of G6PD Mediterranean mutation by amplification refractory mutation system.Semantic proximity Read ↗

[Comparative study of three common G6PD gene mutations in Yao and Han People in Guangxi].Semantic proximity Read ↗

Multiplex primer extension reaction screening and oxidative challenge of glucose-6-phosphate dehydrogenase mutants in hemizygous and heterozygous subjects.Semantic proximity Read ↗

Rapid detection of common Chinese glucose-6-phosphate dehydrogenase (G6PD) mutations by denaturing gradient gel electrophoresis (DGGE).Semantic proximity Read ↗

Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan.Semantic proximity Read ↗

[Identification of three common G6PD gene mutations in Yi minority in Yunnan province].Semantic proximity Read ↗

Large cohort screening of G6PD deficiency and the mutational spectrum in the Dongguan District in Southern China.Semantic proximity Read ↗

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