Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Nov 2004

Francis Jean, Zhang Junhui, Farhi Anita, Carey Hugh, Geller David S

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Aged, 80 and over
Share to Digestive system and related health

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Ion Transport and Channel Regulation

Share to Monosaccharide Transport Proteins

Share to Mutation

Share to Pancreatic function and diabetes

Source

Identifiers

PMID: 15496564
DOI: 10.1093/ndt/gfh426

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria.PMID 15496564Read ↗

Renal glucosuria due to SGLT2 mutationsSemantic proximity Read ↗

A novel sodium-glucose co-transporter 2 gene (SGLT2) mutation contributes to the abnormal expression of SGLT2 in renal tissues in familial renal glucosuria.Semantic proximity Read ↗

Molecular analysis of the SGLT2 gene in patients with renal glucosuria.Semantic proximity Read ↗

Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients.Semantic proximity Read ↗

A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria.Semantic proximity Read ↗

Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).Semantic proximity Read ↗

Genetic analysis and literature review of Chinese patients with familial renal glucosuria: Identification of a novel SLC5A2 mutation.Semantic proximity Read ↗

SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families.Semantic proximity Read ↗

Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.Semantic proximity Read ↗

Search for a Functional Genetic Variant Mimicking the Effect of SGLT2 Inhibitor Treatment.Semantic proximity Read ↗

Familial renal glucosuria: a clinicogenetic study of 23 additional cases.Semantic proximity Read ↗

Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.