ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR322/064/SRR32280564/SRR32280564_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR322/064/SRR32280564/SRR32280564_1.fastq.gzprimary200OKGenomicsPediatrics Department of Hainan Provincial People's Hospitalhttps://www.ebi.ac.uk/ena/browser/view/PRJNA1221317A novel heterozygous mutation in the gelsolin gene causes Finnish gelsolin amyloidosis associated with nephropathy and thrombotic microangiopathyENAfalseA novel heterozygous mutation in the gelsolin gene causes Finnish gelsolin amyloidosis associated with nephropathy and thrombotic microangiopathy2025-02-122025-02-12PRJNA1221317