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

Glucose-6-phosphate dehydrogenase qingzhen: identification of a novel splice mutation (IVS5-1 G>A).

Pediatric blood & cancer - 1 May 2012

Liu Wei-Liang, Li Fang, He Zhi-Xu, Jiang Hong-Yu, Ai Rong

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Glucosephosphate Dehydrogenase
Share to Glucosephosphate Dehydrogenase Deficiency
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 21989994
DOI: 10.1002/pbc.23345

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Glucose-6-phosphate dehydrogenase qingzhen: identification of a novel splice mutation (IVS5-1 G>A).PMID 21989994Read ↗

A synonymous mutation of ancient origin in the glucose-6-phosphate dehydrogenase gene and assessment of haplotypes.Semantic proximity Read ↗

[Identification of glucose-6-phosphate dehydrogenase gene variants in Guangdong populations].Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency: a historical perspectiveSemantic proximity Read ↗

Novel splice-site mutation c.1615-2A>G (IVS14-2A>G) in the SLC26A4 gene causing Pendred syndrome in a consanguineous Portuguese family.Semantic proximity Read ↗

Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene.Semantic proximity Read ↗

A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family.Semantic proximity Read ↗

A novel ALDH5A1 mutation in a patient with succinic semialdehyde dehydrogenase deficiency.Semantic proximity Read ↗

Identification of a case of glucose-6-phosphate dehydrogenase deficiency with G6PD Mediterranean-Middle East subtype in China.Semantic proximity Read ↗

Identification of a case of SRD5A3-congenital disorder of glycosylation (CDG1Q) by exome sequencing.Semantic proximity Read ↗

A novel beta-thalassemia mutation [IVS-II-5 (G-->C)] in a Chinese family from Guangxi Province, P.R. China.Semantic proximity Read ↗

Splice junction [IVS-II-1 (G-->C)] thalassemia; a new mutation detected in an Iranian patient.Semantic proximity Read ↗

Fructose 1,6 bisphosphatase deficiency: outcomes of patients in a single center in Turkey and identification of novel splice site and indel mutations in FBP1.Semantic proximity Read ↗

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