Congenital glucose–galactose malabsorption: a novel deletion within the SLC5A1 gene (Q57150147)

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9 February 2020

title

Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene (English)

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9 February 2020

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Stephanie Van Biervliet

2

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9 February 2020

Bart L Loeys

4

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9 February 2020

author name string

L Vallaeys

1

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9 February 2020

G De Bruyn

3

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A S Moring

5

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E Van Deynse

6

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L Cornette

7

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publication date

29 July 2012

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European Journal of Pediatrics

9 February 2020

published in

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volume

172

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9 February 2020

page(s)

409-411

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issue

3

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https://scigraph.springernature.com/pub.10.1007/s00431-012-1802-9

9 February 2020

exact match

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cites work

A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption

1 reference

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BK virus-associated renal problems--clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1802-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1802-9

Biology of human sodium glucose transporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1802-9

Intestinal absorption in health and disease--sugars

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-012-1802-9

Congenital selective malabsorption of glucose and galactose

21 January 2018

1 reference

12 December 2020

D28G mutation in congenital glucose-galactose malabsorption

1 reference

12 December 2020

Structure and function of the Na+/glucose cotransporter.

1 reference

12 December 2020

Neonatal nephrocalcinosis in association with glucose-galactose malabsorption

1 reference

12 December 2020

10.1007/S00431-012-1802-9

Identifiers

DOI

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9 February 2020

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