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Pathogenesis and laboratory diagnosis of hereditary angioedema

Pathogenesis and laboratory diagnosis of hereditary angioedema

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_citationtrail_10_2500_aap_2009_30_3277

Pathogenesis and laboratory diagnosis of hereditary angioedema

About this item

Full title

Pathogenesis and laboratory diagnosis of hereditary angioedema

Publisher

United States: OceanSide Publications, Inc

Journal title

Allergy and asthma proceedings, 2009-09, Vol.30 (5), p.487-492

Language

English

Formats

Publication information

Publisher

United States: OceanSide Publications, Inc

More information

Scope and Contents

Contents

Hereditary angioedema (HAE) was first described in the 19th century. Over the past 50 years, many details of the pathophysiology and molecular biology of HAE have been elucidated. Two types of HAE, type I and type II, result from mutations in the gene for the broad-spectrum protease
inhibitor C1 inhibitor (C1INH). Type I HAE is characterized by...

Alternative Titles

Full title

Pathogenesis and laboratory diagnosis of hereditary angioedema

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_crossref_citationtrail_10_2500_aap_2009_30_3277

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_citationtrail_10_2500_aap_2009_30_3277

Other Identifiers

ISSN

1088-5412

E-ISSN

1539-6304

DOI

10.2500/aap.2009.30.3277

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