A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F21%3A00120209" target="_blank" >RIV/00216224:14110/21:00120209 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients.
Original language description
A spectrum of SERPING1 mutations and clinical characterisation of Czech Hereditary Angioedema patients - 12th C1-inhibitor deficiency and angioedema workshop 2021 abstract.
Czech name
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Czech description
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Classification
Type
O - Miscellaneous
CEP classification
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OECD FORD branch
30102 - Immunology
Result continuities
Project
<a href="/en/project/NV18-05-00330" target="_blank" >NV18-05-00330: Genetic determination of bradykinin-mediated angioedema severity in patients with hereditary angioedema</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů