Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis (Q35194408)

7 August 2017

title

Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis (English)

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glucose-6-phosphate dehydrogenase deficiency

7 August 2017

main subject

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author name string

Calabrò V

1

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7 August 2017

Mason PJ

2

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7 August 2017

Filosa S

3

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7 August 2017

Civitelli D

4

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7 August 2017

Cittadella R

5

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7 August 2017

Tagarelli A

6

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7 August 2017

Martini G

7

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7 August 2017

Brancati C

8

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7 August 2017

Luzzatto L

9

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7 August 2017

language of work or name

English

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publication date

1 March 1993

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

52

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7 August 2017

issue

3

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7 August 2017

page(s)

527-536

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Genetic diversity of the "Mediterranean" glucose-6-phosphate dehydrogenase deficiency phenotype

7 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Erythrocytic glucose-6-phosphate dehydrogenase measured by a differential pH technique.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Two point mutations are responsible for G6PD polymorphism in Sardinia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Molecular heterogeneity of glucose-6-phosphate dehydrogenase A-.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on a population from the Matera district

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

The genetics of glucose-6-phosphate dehydrogenase deficiency.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Glucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a study on the population of the Cosenza province

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

The molecular basis of glucose-6-phosphate dehydrogenase deficiency

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

Comparison of GdA and GdB activities in Nigerians. A study of the variation of the G6PD activity

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682169

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

13 July 2018

1 reference

12 December 2020

Standardization of hemoglobinometry II. The hemiglobincyanide method

1 reference

12 December 2020

Molecular heterogeneity underlying the G6PD Mediterranean phenotype

1 reference

12 December 2020

Glucose-6-Phosphate Dehydrogenase Lodi^844C: A Study on Its Expression in Blood Cells and Muscle

1 reference

12 December 2020

Seattle variant of glucose-6-phosphate dehydrogenase

1 reference

12 December 2020

Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in Sardinia

1 reference

12 December 2020

Thalassemia types in Calabria (Southern Italy)

1 reference

12 December 2020

Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on the population of Naples

1 reference

12 December 2020

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

12 December 2020

Identifiers

PMC publication ID

1682169

1 reference

7 August 2017

1 reference