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

First molecular confirmation of an Australian case of type III hereditary angioedema.

Pathology - 1 Jan 2008

Bell Christopher G, Kwan Edward, Nolan Richard C, Baumgart Karl W

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 Amino Acid Sequence
Share to Angioedemas, Hereditary
Share to Australia
Share to Base Sequence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Complement C1 Inactivator Proteins

Share to Complement C1 Inhibitor Protein

Share to Molecular Sequence Data

Share to Serpins

Source

Identifiers

PMID: 18038321
DOI: 10.1080/00313020701716433

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

First molecular confirmation of an Australian case of type III hereditary angioedema.PMID 18038321Read ↗

Molecular diagnosis of inherited skin diseases: the paradigm of dystrophic epidermolysis bullosa.Semantic proximity Read ↗

New insights into hereditary angio-oedema: Molecular diagnosis and therapy.Semantic proximity Read ↗

Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations).Semantic proximity Read ↗

Bradykinin-Mediated Angioedema: An Update of the Genetic Causes and the Impact of GenomicsSemantic proximity Read ↗

Hereditary angioedema classification: Expanding knowledge by genotyping and endotypingSemantic proximity Read ↗

In Silico Analysis and In-depth Assessment of a Female Patient with a Missense Mutation in the F12 Gene Associated with Hereditary Angioedema Symptoms: A Case StudySemantic proximity Read ↗

Clinical Utility Gene Card for hereditary angioedema with normal C1 inhibitor (HAEnC1).Semantic proximity Read ↗

International Consensus on the Use of Genetics in the Management of Hereditary AngioedemaSemantic proximity Read ↗

Genetic Analysis as a Practical Tool for Diagnosis of Hereditary Angioedema With Normal C1 Inhibitor: A Case Report.Semantic proximity Read ↗

Type II hereditary angioedema with an apparently de novo SERPING1 mutation in China: A case report and family screening.Semantic proximity Read ↗

Presymptomatic genetic diagnosis of two siblings with hereditary angioedema, presenting with unusual normal levels of serum C4.Semantic proximity Read ↗

Clinical, biochemical, and genetic characterization of a novel estrogen-dependent inherited form of angioedemaSemantic proximity Read ↗

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