ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/067/SRR25619067/SRR25619067_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/059/SRR25619059/SRR25619059_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/063/SRR25619063/SRR25619063_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/057/SRR25619057/SRR25619057_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/065/SRR25619065/SRR25619065_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/060/SRR25619060/SRR25619060_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/066/SRR25619066/SRR25619066_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/065/SRR25619065/SRR25619065_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/061/SRR25619061/SRR25619061_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/062/SRR25619062/SRR25619062_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/059/SRR25619059/SRR25619059_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/058/SRR25619058/SRR25619058_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/066/SRR25619066/SRR25619066_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/064/SRR25619064/SRR25619064_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/063/SRR25619063/SRR25619063_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/062/SRR25619062/SRR25619062_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/067/SRR25619067/SRR25619067_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/064/SRR25619064/SRR25619064_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/058/SRR25619058/SRR25619058_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/057/SRR25619057/SRR25619057_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/061/SRR25619061/SRR25619061_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR256/060/SRR25619060/SRR25619060_1.fastq.gzprimaryOK200GenomicsHangzhou Normal Universityhttps://www.ebi.ac.uk/ena/browser/view/PRJNA1000907we conducted whole-exome sequencing on 12 individuals who have Dystrophic epidermolysis bullosa pruriginosa to identify genetic causing.xref:EuropePMC:PMC10562958ENAfalseWES for DEB disease2023-08-182023-08-18PRJNA1000907