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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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Detalhes bibliográficos
Main Authors: Perfetti, Vittorio, Coluccia, Addolorata M. L., Intini, Daniela, Malgeri, Ursula, Vignarelli, Maurizio Colli, Casarini, Simona, Merlini, Giampaolo, Neri, Antonino
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2001
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1891955/
https://ncbi.nlm.nih.gov/pubmed/11337357
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