BIRSA 101 Breakthrough | India’s First Gene Therapy to CURE Sickle Cell? | NEXT IAS
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BIRSA 101 Breakthrough | India’s First Gene Therapy to CURE Sickle Cell? | NEXT IAS
India has achieved a major milestone in biotechnology with the launch of BIRSA 101, its first indigenous CRISPR-based gene therapy for sickle cell disease. Unlike traditional treatments that only manage symptoms, this one-time therapy targets the root genetic mutation and enables the body to produce healthy red blood cells—offering the ...
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