An ex vivo test to investigate genetic factors conferring susceptibility to atypical haemolytic uremic syndrome

INTRODUCTION: Comprehensive genetic analysis is essential to clinical care of patients with atypical haemolytic uremic syndrome (aHUS) to reinforce diagnosis, and to guide treatment. However, the characterization of complement gene variants remains challenging owing to the complexity of functional s...

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Detalles Bibliográficos
Autores principales: Gastoldi, Sara, Aiello, Sistiana, Galbusera, Miriam, Breno, Matteo, Alberti, Marta, Bresin, Elena, Mele, Caterina, Piras, Rossella, Liguori, Lucia, Santarsiero, Donata, Benigni, Ariela, Remuzzi, Giuseppe, Noris, Marina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949374/
https://www.ncbi.nlm.nih.gov/pubmed/36845135
http://dx.doi.org/10.3389/fimmu.2023.1112257

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949374/
https://www.ncbi.nlm.nih.gov/pubmed/36845135
http://dx.doi.org/10.3389/fimmu.2023.1112257

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