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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...
Guardat en:
| Publicat a: | J Clin Immunol |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer US
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7142058/ https://ncbi.nlm.nih.gov/pubmed/32152940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10875-020-00766-x |
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