Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting (Q28300488)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

José Rueff

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

José Rueff

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

Loeffler J

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Sakallioglu O

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Gok F

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Lhotta K

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Barata J

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

language of work or name

English

0 references

publication date

1 March 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

69

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

page(s)

852-855

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

Molecular Analysis of the SGLT2 Gene in Patients with Renal Glucosuria

17 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

The human kidney low affinity Na+/glucose cotransporter SGLT2. Delineation of the major renal reabsorptive mechanism for D-glucose

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Renal Na(+)-glucose cotransporters

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Renal glucosuria due to SGLT2 mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

The sodium/glucose cotransport family SLC5

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Membrane topology motifs in the SGLT cotransporter family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Cloning of a human kidney cDNA with similarity to the sodium-glucose cotransporter

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Molecular basis for glucose-galactose malabsorption

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Long-term outcome of renal glucosuria type 0: the original patient and his natural history

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5000194

7 January 2021

Identifiers

DOI

10.1038/SJ.KI.5000194

2 references

Consolidated OpenCitations Corpus – April 2017

3350075

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

17 January 2020

1036101184

0 references

3350075

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3350075

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16518345%20AND%20SRC:MED&resulttype=core&format=json