(Q28142013)

English

Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome

scientific article (publication date: November 2000)

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Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome (English)

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O Sakamoto

1

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E Ogawa

series ordinal

2

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T Ohura

series ordinal

3

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Y Igarashi

series ordinal

4

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Y Matsubara

series ordinal

5

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K Narisawa

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6

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K Iinuma

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7

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language of work or name

English

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publication date

November 2000

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published in

Pediatric Research

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volume

48

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issue

5

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page(s)

586-9

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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

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Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Cloning and functional expression of a human pancreatic islet glucose-transporter cDNA.

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Early diabetes and abnormal postnatal pancreatic islet development in mice lacking Glut-2

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Facilitative glucose transporters

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stated in

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reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

C-terminal truncated glucose transporter is locked into an inward-facing form without transport activity

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Fanconi-Bickel syndrome presenting in neonatal screening for galactosaemia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-200011000-00005

retrieved

21 January 2018

Identifiers

DOI

10.1203/00006450-200011000-00005

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Dimensions Publication ID

1003545598

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PubMed publication ID

11044475

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ResearchGate publication ID

12280956

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(Q28142013)

Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome

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