(Q84229596)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21625891%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

Fanconi-Bickel syndrome in a 3-year-old Indian boy with a novel mutation in the GLUT2 gene (English)

1 reference

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2 February 2020

1

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2 February 2020

author name string

Manish Kumar

2

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2 February 2020

Sriram Krishnamurthy

3

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2 February 2020

Osamu Sakamoto

4

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2 February 2020

Sadagopan Srinivasan

5

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2 February 2020

publication date

31 May 2011

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21625891%20AND%20SRC:MED&resulttype=core&format=json

Clinical and experimental nephrology

2 February 2020

published in

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2 February 2020

volume

15

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2 February 2020

issue

5

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2 February 2020

page(s)

745-748

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https://scigraph.springernature.com/pub.10.1007/s10157-011-0456-7

2 February 2020

exact match

0 references

cites work

Fanconi-Bickel syndrome--the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature

1 reference

12 December 2020

[Glucose transport hereditary diseases]

1 reference

12 December 2020

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome

1 reference

12 December 2020

Fanconi-Bickel syndrome.

1 reference

12 December 2020

Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease

1 reference

12 December 2020

No mutation in the SLC2A2 (GLUT2) gene in a Turkish infant with Fanconi-Bickel syndrome

1 reference

12 December 2020

Fanconi-Bickel syndrome

1 reference

12 December 2020

A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome.

1 reference

12 December 2020

Fanconi-Bickel syndrome--a congenital defect of facilitative glucose transport

1 reference

12 December 2020

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

12 December 2020

A fast boosting-based screening method for large-scale association study in complex traits with genetic heterogeneity.

1 reference

12 December 2020

Normal liver, spleen, and kidney dimensions in neonates, infants, and children: evaluation with sonography.

1 reference

12 December 2020

Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome.

1 reference

12 December 2020

GLUT2 mutations, translocation, and receptor function in diet sugar managing

1 reference

12 December 2020

10.1007/S10157-011-0456-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21625891%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

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