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Hereditary Renal Amyloidosis Associated With a Novel Apolipoprotein A-II Variant

Prokaeva, Tatiana
Akar, Harun
Spencer, Brian
Havasi, Andrea
Cui, Haili
O'Hara, Carl J.
Gursky, Olga
Leszyk, John D.
Steffen, Martin
Browning, Sabrina
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Abstract

Here, we report a family with renal amyloidosis associated with a novel stop codon mutation in APOA2 and the apoA-II variant, 78Leuext21.

Source

Kidney Int Rep. 2017 Jul 29;2(6):1223-1232. doi: 10.1016/j.ekir.2017.07.009. eCollection 2017 Nov. Link to article on publisher's site

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DOI
10.1016/j.ekir.2017.07.009
PubMed ID
29270531
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Copyright 2017 International Society of Nephrology. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).