What is SCID-X1? Where is the defect located? - CORRECT ANSWER-More than half

the cases are X-linked. In the commonest of these (SCID-X1), the defect is in the gene

for the gamma chain that forms part of the receptors for IL-2 (Th1 secretes IL-2, which

helps CTL (killer T cells) get fully activated after they recognize antigen.) and other

growth factors necessary for lymphoid development, or their signaling pathways.

What is the other mode of inheritance (not X linked) for people with SCID?...
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