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Article

Early infantile onset of atypical hemolytic-uremic syndrome is caused by recessive mutations in DGKE.

Clinical genetics - 1 Oct 2013

Lee J W

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Share to Diacylglycerol Kinase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 23875923
DOI: 10.1111/cge.12240

Genes

DGKE

Provenance

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

Related research

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Early infantile onset of atypical hemolytic-uremic syndrome is caused by recessive mutations in DGKE.PMID 23875923Read ↗

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

Atypical hemolytic uremic syndrome due to DGKE mutation and response to eculizumab: lessons for the clinical nephrologist.Semantic proximity Read ↗

DGKE and atypical HUS.Semantic proximity Read ↗

Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients.Semantic proximity Read ↗

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

Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years.Semantic proximity Read ↗

Various phenotypes of disease associated with mutated DGKE gene.Semantic proximity Read ↗

Pediatric Atypical Hemolytic Uremic Syndrome Advances.Semantic proximity Read ↗

Phenotypic expansion of DGKE-associated diseases.Semantic proximity Read ↗

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome.Semantic proximity Read ↗

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

Natural history of deoxyguanosine kinase deficiency.Semantic proximity Read ↗

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