Immunoglobulin light chain (AL) amyloidosis is a rare plasma cell dyscrasia characterized by the deposition of abnormal amyloid fibrils in multiple organs. thus impairing their function. In the largest cohort studied up to now of 118 CD138-purified plasma cell samples from previously untreated immunoglobulin light chain amyloidosis patients. we assessed in parallel copy number alterat... https://www.roneverhart.com/Western-Digital-Ultrastar-DC-HC530-WUH721414ALE6L1-0F31170-14TB-7-2K-RPM-SATA-6Gb-s-512e-SED-3-5in-Hard-Drive/