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QJM Advance Access originally published online on February 27, 2006
QJM 2006 99(4):274; doi:10.1093/qjmed/hcl032
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© The Author 2006. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Correspondence

Hereditary renal amyloidosis associated with a novel mutation in the apolipoprotein AII gene

The first 10% of the full text of this article appears below.

Sir,

Hereditary amyloidosis is a rare disorder associated with mutations encoding seven proteins: transthyretin, apolipoproteins AI and AII, gelsolina, cystatin C, lysozyme and fibrinogen A. We report a case of renal amyloidosis affecting . . . [Full Text of this Article]

R. De Gracia, E.J. Fernández, C. Riñón, R. Selgas and J. Garcia-Bustos

Department of Nephrology Department of Haematology University Hospital La Paz Madrid Spain

email: raqueldegracia@yahoo.es


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