Molecular Abnormalities and Diagnosis of Hereditary Leukocyte Disorders (Part 1)
Lu Xingguo Ye Xiangjun (2)T−B− SCID 1. Recombinase-activating Genes1 and 2 Deficiency Recombinase-activating genes1 and 2 (recombinase-activating genes 1 and 2，RAG1/2) deficiency accounts for approximately6% of SCID patients. In about75% of patients with RAG1/2 deficiency, there are very low numbers of T, B lymphocytes, and NK cells. This type of SCID is caused by mutations … Read more