Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis a...
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Scope and Contents
Contents
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare disease. Few states in developing countries have an adequate management of HAE, but none of them belongs to the former USSR area. This study analyses data from C1-INH-HAE patients from Belarus.
Data about clinical characteristics, genetics, access to diagnosis and treatm...
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Full title
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_2bdbd634c5f04df49a6a4ca22be184ec
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2bdbd634c5f04df49a6a4ca22be184ec
Other Identifiers
ISSN
1476-7961
E-ISSN
1476-7961
DOI
10.1186/s12948-021-00141-0
