ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR144/030/SRR14454930/SRR14454930.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR146/006/SRR14665106/SRR14665106.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR146/004/SRR14665104/SRR14665104.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR144/031/SRR14454931/SRR14454931.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR146/010/SRR14665110/SRR14665110.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR146/009/SRR14665109/SRR14665109.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR146/005/SRR14665105/SRR14665105.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR146/008/SRR14665108/SRR14665108.fastq.gzftp://primaryOK200GenomicsCHU Mongi Slimhttps://www.ebi.ac.uk/ena/browser/view/PRJNA727732KIN results from mutations in FAN1 (FANCD2/FANCI-Associated Nuclease 1), a gene involved in the DNA damage response pathway, particularly in the kidney. In this study, we report two Tunisian consanguineous families with KIN caused by mutations in the FAN1 gene.ENAfalseFAN1 sequencing2023-05-192021-05-10PRJNA727732