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Table1_CRISPR/Cas-Based Gene Editing Strategies for DOCK8 I..:
Sujan Ravendran
;
Sabina Sánchez Hernández
;
Saskia König
.
doi:10.3389/fgeed.2022.793010.s001. , 2022
Link:
https://doi.org/10.3389/fgeed.2022.793010.s001
RT Journal T1
Table1_CRISPR/Cas-Based Gene Editing Strategies for DOCK8 Immunodeficiency Syndrome.xlsx
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_19374767&Exemplar=1&LAN=DE A1 Sujan Ravendran A1 Sabina Sánchez Hernández A1 Saskia König A1 Rasmus O. Bak YR 2022 K1 Genetics K1 Molecular Biology K1 Genetic Engineering K1 Molecular Medicine K1 Gene and Molecular Therapy K1 gene editing (CRISPR-Cas9) K1 CRISPR/Cas 9 K1 hematopoietic stem cell K1 DOCK8 immunodeficiency syndrome K1 DOCK8 deficiency K1 DOCK8 K1 gene therapy K1 Primary immunodeficiency JF doi:10.3389/fgeed.2022.793010.s001 LK http://dx.doi.org/https://doi.org/10.3389/fgeed.2022.793010.s001 DO https://doi.org/10.3389/fgeed.2022.793010.s001 SF ELIB - SuUB Bremen
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