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

Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Sept 2010

Godefroid Nathalie, Dahan Karin

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 NPHS1 gene
Share to Genotype
Share to Membrane Proteins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nephrotic Syndrome

Share to Phenotype

Source

Identifiers

PMID: 20650908
DOI: 10.1093/ndt/gfq434

Genes

NPHS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.PMID 20650908Read ↗

Expanding the spectrum of NPHS1-associated disease.Semantic proximity Read ↗

A case report of congenital nephrotic syndrome caused by new mutations of NPHS1.Semantic proximity Read ↗

Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic CounselingSemantic proximity Read ↗

[Congenital nephrotic syndrome].Semantic proximity Read ↗

Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome.Semantic proximity Read ↗

Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type.Semantic proximity Read ↗

Novel NPHS1 Gene Mutations in two Chinese Infants with Congenital Nephrotic Syndrome.Semantic proximity Read ↗

Congenital nephrotic syndrome.Semantic proximity Read ↗

Prenatal diagnosis of congenital nephrotic syndrome (CNF, NPHS1).Semantic proximity Read ↗

NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.Semantic proximity Read ↗

Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS).Semantic proximity Read ↗

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.Semantic proximity Read ↗

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