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

Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in Singapore Chinese.

American journal of hematology - 1 Dec 1994

Saha S, Saha N, Tay J S, Jeyaseelan K, Basair J B, Chew S E

Abstract excerpt

Sixty-two G6PD deficient Chinese males have been investigated for the presence of seven mutations of the coding region of the G6PD gene by natural and artificially created amplified restriction sites. The results show that the G to T substitution at nucleotide (nt) 1376 and G to A substitution at nt 1388 represent 24% and 21% of G6PD deficiency, respectively, in the Singapore Chinese; 37% of the sample could not...

Read the complete abstract on PubMed

Topics

Base Sequence
China
DNA Primers
Genes
Glucosephosphate Dehydrogenase Deficiency
Humans
Male

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Molecular Sequence Data

Mutation

Singapore

Source

Identifiers

PMID: 7977299
DOI: 10.1002/ajh.2830470405

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in Singapore Chinese.PMID 7977299Read ↗

Biochemical characteristics of four common molecular variants in glucose-6-phosphate dehydrogenase-deficient Chinese in Singapore.Semantic proximity Read ↗

Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in patients of Chinese descent and identification of new base substitutions in the human G6PD geneSemantic 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 ↗

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

Complete molecular characterisation of glucose-6-phosphate dehydrogenase (G6PD) deficiency in a group of Malaysian Chinese neonates.Semantic proximity Read ↗

Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.Semantic proximity Read ↗

Two new variants of G6PD deficiencies in Singapore.Semantic proximity Read ↗

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

Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in north-west Pakistan.Semantic proximity Read ↗

Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype-phenotype and description of a new variant (G6PD Neapolis).Semantic proximity Read ↗

Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361A.Semantic proximity Read ↗

Molecular characterization of G6PD deficiency in Cyprus.Semantic proximity Read ↗

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