{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR112/083/SRR11252083/SRR11252083_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR112/083/SRR11252083/SRR11252083_2.fastq.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["The First Affiliated Hospital of Shenzhen University"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA610829"],"long_description":["The whole-exome sequencing to identify missense variants in a patient with SCAD"],"repository":["ENA"],"description_synonyms":["deficiency OF, lipid-storage myopathy secondary to short-chain acyl-Coa dehydrogenase deficiency, Acads deficiency, short-chain acyl-coenzyme A dehydrogenase deficiency, Scadh deficiency, ACADSD, Bcd1, Hdlq8, Scad deficiency, short-chain acyl-CoA dehydrogenase deficiency, Scad, short-chain, SCAD, acyl-CoA dehydrogenase, 1.3.8.1, Bcd-1, ACAD3., Butyryl-CoA dehydrogenase, AI196007"],"additional_accession":[]},"is_claimable":false,"name":"","description":"SCAD variant sequencing","dates":{"last_updated":"2023-05-19","first_public":"2020-03-24"},"accession":"PRJNA610829","cross_references":{}}