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

A multiplex method for detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations.

International journal of laboratory hematology - 1 Dec 2015

Zhang L, Yang Y, Liu R, Li Q, Yang F, Ma L, Liu H, Chen X, Yang Z, Cui L, He Y

Abstract excerpt

INTRODUCTION: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect caused by G6PD gene mutations. This study aimed to develop a cost-effective, multiplex, genotyping method for detecting common mutations in the G6PD gene. METHODS: We used a SNaPshot approach...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to DNA Mutational Analysis
Share to Genotyping Techniques

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Multiplex Polymerase Chain Reaction

Share to Mutation

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 26190099
DOI: 10.1111/ijlh.12405
PMCID: PMC4715770

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-26190099-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A multiplex method for detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations.PMID 26190099Read ↗

Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency at the China-Myanmar Border.Semantic proximity Read ↗

Rapid detection of glucose-6-phosphate dehydrogenase gene mutations by denaturing high-performance liquid chromatography.Semantic proximity Read ↗

Multiplex Snapshot minisequencing for the detection of common PAH gene mutations in Iranian patients with PhenylketonuriaSemantic proximity Read ↗

Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.Semantic proximity Read ↗

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

Distribution of G6PD deficiency genotypes among Southeast Asian populationsSemantic proximity Read ↗

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

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

Rapid, simultaneous genotyping of 10 Southeast Asian glucose-6-phosphate dehydrogenase deficiency-causing mutations and a silent polymorphism by multiplex primer extension/denaturing HPLC assay.Semantic proximity Read ↗

A capillary electrophoresis-based variant hotspot genotyping method for rapid and reliable analysis of the phenylalanine hydroxylase gene in the Chinese Han population.Semantic proximity Read ↗

Designing primers for SNaPshot technique.Semantic proximity Read ↗

Incidence and molecular characterization of Glucose-6-Phosphate Dehydrogenase deficiency among neonates for newborn screening in Chaozhou, China.Semantic proximity Read ↗

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