Cargando…
Hereditary C2 deficiency: Genetic studies and association with the HL-A system
Herediatary C2-deficiency has been shown to be transmitted asn an autosomal recessive characteristic. Recent evidence indicates that some genetic factors involved in the control of the complement (C) system in both man and mice are governed by genes localized within the major histocompatibility regi...
Formato: | Texto |
---|---|
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1975
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189860/ https://www.ncbi.nlm.nih.gov/pubmed/1127385 |
Ejemplares similares
-
Post-vaccine glomerulonephritis in an infant with hereditary C2 complement deficiency: case study
por: Kersnik Levart, Tanja
Publicado: (2013) -
Clinical and genetic features of hereditary angioedema with and without C1‐inhibitor (C1‐INH) deficiency in Japan
por: Hashimura, Chinami, et al.
Publicado: (2021) -
Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)
por: Parsopoulou, Faidra, et al.
Publicado: (2022) -
Secreted Phospholipases A(2) in Hereditary Angioedema With C1-Inhibitor Deficiency
por: Loffredo, Stefania, et al.
Publicado: (2018) -
Pediatric hereditary angioedema due to C1-inhibitor deficiency
por: Farkas, Henriette
Publicado: (2010)