(Q35716837)

9 August 2017

0 references

A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe (English)

1 reference

9 August 2017

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1 reference

Walid Fazeli

1

1 reference

9 August 2017

Sigrid Kaczmarek

series ordinal

2

1 reference

9 August 2017

Martin Kirschstein

series ordinal

3

1 reference

9 August 2017

René Santer

series ordinal

4

1 reference

9 August 2017

language of work or name

1 reference

28 July 2015

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9 August 2017

1 reference

9 August 2017

15

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9 August 2017

90

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Creative Commons Attribution 4.0 International

9 August 2017

start time

28 July 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/s12876-015-0316-0

0 references

cites work

Two novel mutations in the lactase gene in a Japanese infant with congenital lactase deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Impaired trafficking and subcellular localization of a mutant lactase associated with congenital lactase deficiency

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Clinical significance of enzymatic deficiencies in the gastrointestinal tract with particular reference to lactase deficiency

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Congenital lactose intolerance is triggered by severe mutations on both alleles of the lactase gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Molecular genetics of human lactase deficiencies

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Nephrolithiasis in a child with glucose-galactose malabsorption

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4515929

Congenital lactase deficiency

25 September 2018

1 reference

12 December 2020

[Idiopathic lactosuria in a patient of chronic diarrhea and acidosis.]

1 reference

12 December 2020

METHOD FOR ASSAY OF INTESTINAL DISACCHARIDASES

1 reference

12 December 2020

Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency

1 reference

12 December 2020

10.1186/S12876-015-0316-0

Identifiers

DOI

1 reference

9 August 2017

1 reference

9 August 2017

1 reference