Complement Activation in 22q11.2 Deletion Syndrome

The 22q11.2 deletion syndrome (22q11.2 del), also known as DiGeorge syndrome, is a genetic disorder with an estimated incidence of 1:3000 to 1:6000 births. These patients may suffer from affection of many organ systems with cardiac malformations, immunodeficiency, hypoparathyroidism, autoimmunity, p...

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Detalles Bibliográficos
Autores principales: Grinde, Dina, Øverland, Torstein, Lima, Kari, Schjalm, Camilla, Mollnes, Tom Eirik, Abrahamsen, Tore G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142058/
https://www.ncbi.nlm.nih.gov/pubmed/32152940
http://dx.doi.org/10.1007/s10875-020-00766-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142058/
https://www.ncbi.nlm.nih.gov/pubmed/32152940
http://dx.doi.org/10.1007/s10875-020-00766-x

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