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

Human properdin deficiency has a heterogeneous genetic background.

Immunopharmacology - 1 Dec 1997

Truedsson L, Westberg J, Fredrikson G N, Sjöholm A G, Kuijper E J, Fijen C A, Späth P J, Uhlén M

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 Chromosome Mapping
Share to Genetic Linkage
Share to Meningococcal Infections
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to X Chromosome

Source

Identifiers

PMID: 9476131
DOI: 10.1016/s0162-3109(97)00087-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human properdin deficiency has a heterogeneous genetic background.PMID 9476131Read ↗

Properdin deficiency: molecular basis and disease association.Semantic proximity Read ↗

[Properdin deficiency].Semantic proximity Read ↗

[Properdin mutations a risk factor for meningitis].Semantic proximity Read ↗

A novel mutation W388X underlying properdin deficiency in a Finnish family.Semantic proximity Read ↗

Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency.Semantic proximity Read ↗

Recurrent meningococcal septicaemia and properdin deficiencySemantic proximity Read ↗

Pathophysiology of Human Genetic CD36 DeficiencySemantic proximity Read ↗

SAMHD1 Mutations Are Also Responsible for Aicardi-Goutières in the Cree Population.Semantic proximity Read ↗

Properdin deficiency and meningococcal disease—identifying those most at riskSemantic proximity Read ↗

Carrier detection in families with properdin deficiency by microsatellite haplotyping.Semantic proximity Read ↗

Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchangeSemantic proximity Read ↗

Lessons to the learned from TBG deficiency.Semantic proximity Read ↗

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