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Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema

Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3075700774

Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema

About this item

Full title

Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema

Publisher

United States: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2024-07, Vol.391 (1), p.56-59

Language

English

Formats

Publication information

Publisher

United States: Massachusetts Medical Society

More information

Scope and Contents

Contents

Hereditary angioedema is a potentially life-threatening autosomal dominant condition, causing attacks of angioedema due to failure to regulate bradykinin. Nearly all cases of hereditary angioedema are caused by mutations in the gene encoding C1 inhibitor,
SERPING1
. C1 inhibitor is a multifunctional protein produced in the liver that regulate...

Alternative Titles

Full title

Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_3075700774

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_3075700774

Other Identifiers

ISSN

0028-4793,1533-4406

E-ISSN

1533-4406

DOI

10.1056/NEJMoa2400403

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