Translocation t(4;14)(p16.3;q32) Is a Recurrent Genetic Lesion in Primary Amyloidosis

Primary amyloidosis is a fatal disorder characterized by low numbers of clonal plasma cells in the bone marrow and the systemic deposition of light chain fragments in the form of amyloid. The molecular pathobiology of amyloidosis is primarily unknown. Recently, a novel karyotypically undetectable t(...

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Bibliografiske detaljer
Main Authors: Perfetti, Vittorio, Coluccia, Addolorata M. L., Intini, Daniela, Malgeri, Ursula, Vignarelli, Maurizio Colli, Casarini, Simona, Merlini, Giampaolo, Neri, Antonino
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Investigative Pathology 2001
Fag:
Short Communications
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1891955/
https://ncbi.nlm.nih.gov/pubmed/11337357
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