Genomics

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Development and IND-enabling studies of a novel Cas9 genome-edited autologous CD34+ cell therapy to induce fetal hemoglobin for sickle cell disease [scRNA]

ABSTRACT: Development and IND-enabling studies of a novel Cas9 genome-edited autologous CD34+ cell therapy to induce fetal hemoglobin for sickle cell disease [scRNA]

PROVIDER: PRJNA1149034 | ENA |

REPOSITORIES: ENA

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Action DRS
SRR30275600.fastq.gz Fastqsanger.gz
SRR30275601.fastq.gz Fastqsanger.gz
SRR30275590.fastq.gz Fastqsanger.gz
SRR30275591.fastq.gz Fastqsanger.gz
SRR30275592.fastq.gz Fastqsanger.gz
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