Familial atypical hemolytic uremic syndrome with positive p.S1191L (c.3572C>T) mutation on the CFH gene: A single-center experience

Categoría del artículo: Original Article

Publicado en línea: 27 jul 2021

Páginas: 81 - 88

DOI: https://doi.org/10.2478/bjmg-2021-0007

Palabras clave

Complement factor H () gene, Eculizumab (ECZ), Familial atypical hemolytic uremic syndrome (aHUS), Plasmapheresis, p.S1191L mutation

© 2021 Ersoy Dursun F, Yesil G, Sasak G, Dursin H, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.