Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene (Q28262225)

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

Primaquine sensitivity. Glucose-6-phosphate dehydrogenase deficiency: an inborn error of metabolism of medical and biological significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

Linkage between Deficiency of Glucose-6-phosphate Dehydrogenase and Colour-blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Glucose-6-phosphate dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Definition of the Mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD ‘Lejeune’

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Some Mexican glucose-6-phosphate dehydrogenase variants revisited

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Glucose-6-phosphate dehydrogenase variants in Hawaii

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

A to G substitution identified in exon 2 of the G6PD gene among G6PD deficient Chinese

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Sequence of human glucose-6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Two commonly occurring nucleotide base substitutions in Chinese G6PD variants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

GENERATION OF HYDROGEN PEROXIDE IN ERYTHROCYTES BY HEMOLYTIC AGENTS.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Human glucose-6-phosphate dehydrogenase: purification of the erythrocyte enzyme and the influence of ions on its activity.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Molecular heterogeneity underlying the G6PD Mediterranean phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Identification of the binding domain for NADP+ of human glucose-6-phosphate dehydrogenase by sequence analysis of mutants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Favism: clinical and biochemical data

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Deficiency in red blood cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

G6PD Canton a common deficient variant in South East Asia caused by a 459 Arg----Leu mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

A single nucleotide base transition is the basis of the common human glucose-6-phosphate dehydrogenase variant A (+).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Glucose-6-phosphate-dehydrogenase deficiency in Nigerians with jaundice associated with lobar pneumonia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Common glucose-6-phosphate dehydrogenase (G6PD) variants from the Italian population: biochemical and molecular characterization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380020302

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380020302

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/l5d6jv34wzhl5nt2yjumxmkhr4

30 July 2022

mapped directly with Wikidata item

Fatcat ID

release_l5d6jv34wzhl5nt2yjumxmkhr4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/l5d6jv34wzhl5nt2yjumxmkhr4

30 July 2022

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

3289003

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3289003

PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/l5d6jv34wzhl5nt2yjumxmkhr4

30 July 2022