Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan (Q72223145)

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24 October 2019

title

Molecular abnormality of G6PD Konan and G6PD Ube, the most common glucose-6-phosphate dehydrogenase variants in Japan (English)

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24 October 2019

author name string

A Hirono

series ordinal

1

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24 October 2019

H Fujii

series ordinal

2

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24 October 2019

S Miwa

series ordinal

3

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24 October 2019

publication date

1 June 1993

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24 October 2019

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24 October 2019

volume

91

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issue

5

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24 October 2019

page(s)

507-508

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https://scigraph.springernature.com/pub.10.1007/bf00217781

24 October 2019

exact match

0 references

cites work

G6PD Ube, a glucose-6-phosphate dehydrogenase variant found in four unrelated Japanese families

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA sequencing with chain-terminating inhibitors

1 reference

12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

12 December 2020

Incidence and characteristics of glucose-6-phosphate dehydrogenase variants in Japan

1 reference

12 December 2020

cDNA cloning of human R-type pyruvate kinase and identification of a single amino acid substitution (Thr384----Met) affecting enzymatic stability in a pyruvate kinase variant (PK Tokyo) associated with hereditary hemolytic anemia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00217781

1 reference

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24 October 2019

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