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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Main Authors: Perfetti, Vittorio, Coluccia, Addolorata M. L., Intini, Daniela, Malgeri, Ursula, Vignarelli, Maurizio Colli, Casarini, Simona, Merlini, Giampaolo, Neri, Antonino
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Society for Investigative Pathology 2001
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Short Communications
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1891955/
https://ncbi.nlm.nih.gov/pubmed/11337357
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