KFU. Card publication. Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene

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HEREDITARY ANGIOEDEMA DUE TO C1 INHIBITOR DEFICIENCY IN BELARUS: EPIDEMIOLOGY, ACCESS TO DIAGNOSIS AND SEVEN NOVEL MUTATIONS IN SERPING1 GENE

Form of presentation

Articles in international journals and collections

Year of publication

2021

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Authors, employees of KFU

Belevcev Mikhail Vladimirovich, author

Guryanova Irina Evgenevna, author

Polyakova Ekaterina Aleksandrovna, author

Bibliographic description in the original language

Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene /Guryanova, I., Suffritti, C., Parolin, D. et al. Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene// Clin Mol Allergy 19, 3 (2021). https://doi.org/10.1186/s12948-021-00141-0

Keywords

Hereditary angioedem�, C1 inhibitor deficiency, novel mutations in SERPING1 gene

The name of the journal

Clinical and Molecular Allergy

Please use this ID to quote from or refer to the card

https://repository.kpfu.ru/eng/?p_id=271487&p_lang=2

Resource files

File name	Size (MB)	Format
s12948_021_00141_0__1_.pdf	1,00	pdf	show / download

Full metadata record

Field DC	Value	Language
dc.contributor.author	Belevcev Mikhail Vladimirovich	ru_RU
dc.contributor.author	Guryanova Irina Evgenevna	ru_RU
dc.contributor.author	Polyakova Ekaterina Aleksandrovna	ru_RU
dc.date.accessioned	2021-01-01T00:00:00Z	ru_RU
dc.date.available	2021-01-01T00:00:00Z	ru_RU
dc.date.issued	2021	ru_RU
dc.identifier.citation	Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene /Guryanova, I., Suffritti, C., Parolin, D. et al. Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene// Clin Mol Allergy 19, 3 (2021). https://doi.org/10.1186/s12948-021-00141-0	ru_RU
dc.identifier.uri	https://repository.kpfu.ru/eng/?p_id=271487&p_lang=2	ru_RU
dc.description.abstract	Clinical and Molecular Allergy	ru_RU
dc.language.iso	ru	ru_RU
dc.subject	Hereditary angioedem�	ru_RU
dc.subject	C1 inhibitor deficiency	ru_RU
dc.subject	novel mutations in SERPING1 gene	ru_RU
dc.title	Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene	ru_RU
dc.type	Articles in international journals and collections	ru_RU