We believe we will have a gene therapy ready to be tested in clinical trials within the next 5 years.” Harnessing CRISP gene editing: the team intends ...
https://www.google.com/url?rct=j&sa=t&url=https://oicanadian.com/congenital-cardiomyopathy-rewriting-dna-to-erase-heart-disease/&ct=ga&cd=CAIyGmEyNDJjNTAxZWU3OTQyNzI6Y29tOmVuOlVT&usg=AOvVaw1yNjNJ9HMfk6XsKKlt1K5Z
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