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Identification of a novel missense variant in SPDL1 associated with idiopathic pulmonary fibrosis
[article]
2020
bioRxiv
pre-print
Idiopathic pulmonary fibrosis (IPF) is a fatal disorder characterised by progressive, destructive lung scarring. Despite significant progress, the genetic determinants of this disease remain incompletely defined. Using next generation sequencing data from 752 individuals with sporadic IPF and 119,055 controls, we performed both variant- and gene-level analyses to identify novel IPF genetic risk factors. Our variant-level analysis revealed a novel rare missense variant in SPDL1 (NM_017785.5
doi:10.1101/2020.06.29.178079
fatcat:clzlf7jeqvhhbczxstqpm4cx2y