Yüklüyor......
Agammaglobulinemia: from X-linked to Autosomal Forms of Disease
Interruptions or alterations in the B cell development pathway can lead to primary B cell immunodeficiency with resultant absence or diminished immunoglobulin production. While the most common cause of congenital agammaglobulinemia is X-linked agammaglobulinemia (XLA), accounting for approximately 8...
Kaydedildi:
| Yayımlandı: | Clin Rev Allergy Immunol |
|---|---|
| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Springer US
2021
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8269404/ https://ncbi.nlm.nih.gov/pubmed/34241796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12016-021-08870-5 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|