Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene.
Saved in:
| Title: | Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene. |
|---|---|
| Authors: | Guryanova, Irina1 (AUTHOR) guryanovairina1985@gmail.com, Suffritti, Chiara2 (AUTHOR), Parolin, Debora3 (AUTHOR), Zanichelli, Andrea2 (AUTHOR), Ishchanka, Nastassia4 (AUTHOR), Polyakova, Ekaterina1 (AUTHOR), Belevtsev, Mikhail1 (AUTHOR), Perego, Francesca5 (AUTHOR), Cicardi, Marco5 (AUTHOR), Zharankova, Yulia1 (AUTHOR), Konoplya, Natalya1 (AUTHOR), Caccia, Sonia3 (AUTHOR), Gidaro, Antonio2 (AUTHOR) |
| Source: | Clinical & Molecular Allergy. 4/7/2021, Vol. 19 Issue 1, p1-8. 8p. |
| Database: | Academic Search Ultimate |
Be the first to leave a comment!
