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

Genetics: Hidden intronic mutations in DGKE are causative of aHUS.

Nature reviews. Nephrology - 1 Jun 2015

Edwards Jessica K

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 Atypical Hemolytic Uremic Syndrome
Share to Diacylglycerol Kinase
Share to Introns
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 25917558
DOI: 10.1038/nrneph.2015.68

Genes

DGKE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetics: Hidden intronic mutations in DGKE are causative of aHUS.PMID 25917558Read ↗

A common coding variant in BAG3 protects from heart failure.Semantic proximity Read ↗

[Clinical challenges and research progress in variants of uncertain significance of inherited cardiovascular diseases].Semantic proximity Read ↗

A novel compound heterozygous mutation in DGKE in a Chinese patient causes atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Nomenclature for human DPYD alleles.Semantic proximity Read ↗

Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: HEXA. Disease: Tay-Sachs disease.Semantic proximity Read ↗

[Advance of the research for disease-responsible genes].Semantic proximity Read ↗

Genetics: broken giant linked to heart failure.Semantic proximity Read ↗

EAS Consensus Panel statement on homozygous FH.Semantic proximity Read ↗

EDA-ID: a Severe Clinical Presentation Associated with a New IKBKG Mutation.Semantic proximity Read ↗

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.Semantic proximity Read ↗

Atypical haemolytic uraemic syndrome in a Japanese patient with DGKE genetic mutations.Semantic proximity Read ↗

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