Pioneering the future: CRISPR-Cas9 gene therapy for hereditary hemorrhagic telangiectasia.
European journal of internal medicine, 127: 140-141 PMID 38879351 DOI 10.1016/j.ejim.2024.06.012
Abstract
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European journal of internal medicine, 127: 140-141 PMID 38879351 DOI 10.1016/j.ejim.2024.06.012
This article has no abstract in PubMed.