Cargando...

Screening for Plasminogen Mutations in Hereditary Angioedema Patients

Hereditary angioedema (HAE) is a rare disease belonging to the group of bradykinin-mediated angioedemas, characterized by recurring edematous episodes involving the subcutaneous and/or submucosal tissues. Most cases of HAE are caused by mutations in the SERPING1 gene encoding C1-inhibitor (C1-INH-HA...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Genes (Basel)
Main Authors: Farkas, Henriette, Dóczy, Anna, Szabó, Edina, Varga, Lilian, Csuka, Dorottya
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2021
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7998782/
https://ncbi.nlm.nih.gov/pubmed/33799813
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12030402
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!