{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/005/SRR6740275/SRR6740275_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/003/SRR6740273/SRR6740273_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/003/SRR6740273/SRR6740273_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/004/SRR6740274/SRR6740274_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/002/SRR6740272/SRR6740272_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/005/SRR6740275/SRR6740275_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/004/SRR6740274/SRR6740274_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR674/002/SRR6740272/SRR6740272_2.fastq.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["university of Strasbourg"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA434369"],"tag":["xref:EuropePMC:PMC6225799"],"long_description":["The aim of this study was to understand why two siblings carrying both the same homozygous causal mutation for the auto-inflammatory disease hyper IgD syndrome show opposite phenotypes, i.e. the first being asymptomatic, the second presenting all classical characteristics of the disease."],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"","description":"Exome data of Mevalonate kinase deficiency family","dates":{"last_updated":"2023-05-19","first_public":"2018-03-01"},"accession":"PRJNA434369","cross_references":{}}