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Genetic variants of SERPING1 gene in Polish patients with hereditary angioedema due to C1 inhibitor deficiency
Hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE) type I and II is a rare and life-threatening disease caused by SERPING1 gene mutations. Previous genetic studies indicated a wide spectrum of disease-associated variants in the SERPING1 gene and often lack of correlation with patient’...
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| Publicado no: | Cent Eur J Immunol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Termedia Publishing House
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7790005/ https://ncbi.nlm.nih.gov/pubmed/33437182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/ceji.2020.101252 |
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