(Q34719638)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

Glucose-6-phosphate dehydrogenase mutations in Mon and Burmese of southern Myanmar (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

author name string

Chalisa Louicharoen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

Warisa Charoenvej

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

publication date

28 November 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

28 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

volume

53

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

page(s)

48-54

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18046504%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10038-007-0217-3

28 December 2019

exact match

0 references

cites work

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.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-007-0217-3

Further investigations of glucose-6-phosphate dehydrogenase variants in Flores Island, eastern Indonesia

21 January 2018

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Cambodia: G6PD Viangchan (871G>A) is the most common variant in the Cambodian population

1 reference

12 December 2020

Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants

1 reference

12 December 2020

Molecular heterogeneity underlying the G6PD Mediterranean phenotype

1 reference

12 December 2020

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

1 reference

12 December 2020

Coexistence of five G6PD variants indicates ethnic complexity of Phuket islanders, Southern Thailand.

1 reference

12 December 2020

Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese

1 reference

12 December 2020

Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population

1 reference

12 December 2020

The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia.

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Myanmar: G6PD Mahidol (487G>A) is the most common variant in the Myanmar population

1 reference

12 December 2020

Two new mutations of the glucose-6-phosphate dehydrogenase (G6PD) gene associated with haemolytic anaemia: clinical, biochemical and molecular relationships

1 reference

12 December 2020

Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia

1 reference

12 December 2020

Glucose-6 phosphate dehydrogenase mutations and haplotypes in various ethnic groups.

1 reference

12 December 2020

Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind).

1 reference

12 December 2020

Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan.

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group

1 reference

12 December 2020

G6PD Viangchan (871G>A) is the most common G6PD-deficient variant in the Cambodian population.

1 reference

12 December 2020

[Molecular analysis of glucose-6-dehydrogenase deficiency in Spain]

1 reference

12 December 2020

Molecular variants of red cell glucose-6-phosphate dehydrogenase deficiency in Central Java, Indonesia

1 reference

12 December 2020

MALARIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN THAILAND

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Molecular basis of G6PD deficiency in India

1 reference

12 December 2020

Molecular heterogeneity of G6PD deficiency in an Amazonian population and description of four new variants

1 reference

12 December 2020

Glucose-6-phosphate dehydrogenase (G-6-PD) mutations in Mexico: four new G-6-PD variants

1 reference

12 December 2020