The genetic defect-adenosine deaminase $(ADA)$ deficiency may be cured permanently by

  • A
    administering adenosine deaminase activators
  • B
    introducing bone marrow cells producing $ADA$ into cells at early embryonic stages
  • C
    enzyme replacement therapy
  • D
    periodic infusion of genetically engineered lymphocytes having functional $ADA$ $cDNA$

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