Biblio
Crispr-Based Editing of Human Pluripotent Stem Cells for Disease Modeling. Stem Cell Rev Rep. 2024.
. In Vivo Base Editing of Scn5a Rescues Type 3 Long QT Syndrome in Mice. Circulation. 2023.
The establishment of a homozygous SNTA1 knockout human embryonic stem cell line (WAe009-A-50) using the CRISPR/Cas9 system. Stem Cell Res. 2021;51:102196.
. Generation of a TPM1 homozygous knockout embryonic stem cell line by CRISPR/Cas9 editing. Stem Cell Res. 2021;55:102470.
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