India launches 1st indigenous CRISPR-based gene therapy for Sickle Cell Disease
Setting a new milestone, the Indian government on November 20 launched an indigenous CRISPR-based gene therapy for Sickle Cell Disease, which particularly affects India`s tribal population. The low-cost gene editing solution named “BIRSA 101”, in honour of Bhagwan Birsa Munda, remembered as a great tribal freedom fighter, was launched by Union Minister of State […]
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