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 Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene.

The Journal of allergy and clinical immunology - 1 Apr 2009

Büyüköztürk Suna, Eroğlu Belgin Kesim, Gelincik Asli, Uzümcü Abdullah, Ozşeker Ferhan, Colakoğlu Bahattin, Dal Murat, Uyguner Z Oya

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 Angioedemas, Hereditary
Share to Complement C1 Inhibitor Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Promoter Regions, Genetic

Share to RNA, Messenger

Source

Identifiers

PMID: 19201015
DOI: 10.1016/j.jaci.2008.12.022

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Turkish family with a novel mutation in the promoter region of the C1 inhibitor gene.PMID 19201015Read ↗

Newly found C1 inhibitor gene mutation in hereditary angioedema patients.Semantic proximity Read ↗

Molecular genetics of C1 inhibitor.Semantic proximity Read ↗

Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedemaSemantic proximity Read ↗

De novo homozygous mutation of the C1 inhibitor gene in a patient with hereditary angioedema.Semantic proximity Read ↗

Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysisSemantic proximity Read ↗

[C1 inhibitor deficiency].Semantic proximity Read ↗

C1- inhibitors and their genes: an update.Semantic proximity Read ↗

The effect of sequence variations within the coding region of the C1 inhibitor gene on disease expression and protein function in families with hereditary angio-oedema.Semantic proximity Read ↗

Clinical presentations and molecular basis of complement C1R mutation in a large turkish familySemantic proximity Read ↗

C1-inhibitor and its genetic alterations in hereditary angioneurotic edema.Semantic proximity Read ↗

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype AssociationSemantic proximity Read ↗

Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with Inherited Antithrombin DeficiencySemantic proximity Read ↗

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