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The Wall Street Journal

Crispr Gene-Modifying Medicine Present Promise in Preliminary Research

Intellia Therapeutics Inc. reported encouraging early-stage examine outcomes for its Crispr gene-editing remedies, the newest signal that the pathbreaking technology may end in commercially obtainable medicine within the coming years.

Intellia mentioned Friday that one among its remedies, code-named NTLA-2002, considerably decreased ranges of a protein that causes periodic assaults of swelling in six sufferers with a uncommon genetic illness known as hereditary angioedema, or HAE.

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