Answers are grounded in this paper and cite their sources.
TO THE EDITOR: Systemic amyloid light-chain amyloidosis (AL) is characterized by deposition of misfolded immunoglobulin light chains within organs. AL with an immunoglobulin M (IgM) monoclonal protein (IgM-AL) accounts for 5% to 7% of AL and exhibits more prevalent lymph node, neuropathic, and lung
No takes yet. Share an insight, caveat, or question.
Manwani et al. (2018) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: