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CRISPR technology can correct Alpha-1 antitrypsin deficiency

Groundbreaking research demonstrates proof-of-concept for using CRISPR-Cas9 genome editing technology…

4 July 2018 | By Dr Zara Kassam (Drug Target Review)

Groundbreaking research demonstrates proof-of-concept for using CRISPR-Cas9 genome editing technology to correct the gene mutation responsible for AAT deficiency...

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Shen Shen

CRISPR technology can correct Alpha-1 antitrypsin deficiency