ReviewGene therapy2022
Genome editing using CRISPR/Cas9 to treat hereditary hematological disorders.
Yan Chen et al.PubMed ↗Publisher ↗
No numbers read from the abstract.
15 papers cite it
this papercites it
ReviewGene therapy2022
Yan Chen et al.PubMed ↗Publisher ↗
No numbers read from the abstract.