. . . . . . . "[We recently identified the first naturally occurring structural variant, D76N, of human ?2-microglobulin (?2m), the ubiquitous light chain of class I major histocompatibility antigens, as the amyloid fibril protein in a family with a new phenotype of late onset fatal hereditary systemic amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:10:49+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .