Loading...
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
Prokaeva, Tatiana
Akar, Harun
Spencer, Brian
Havasi, Andrea
Cui, Haili
O'Hara, Carl J.
Gursky, Olga
Leszyk, John D.
Steffen, Martin
Browning, Sabrina
Citations
Altmetric:
Authors
Prokaeva, Tatiana
Akar, Harun
Spencer, Brian
Havasi, Andrea
Cui, Haili
O'Hara, Carl J.
Gursky, Olga
Leszyk, John D.
Steffen, Martin
Browning, Sabrina
Rosenberg, Allison
Connors, Lawreen H.
Akar, Harun
Spencer, Brian
Havasi, Andrea
Cui, Haili
O'Hara, Carl J.
Gursky, Olga
Leszyk, John D.
Steffen, Martin
Browning, Sabrina
Rosenberg, Allison
Connors, Lawreen H.
Student Authors
Faculty Advisor
Academic Program
UMass Chan Affiliations
Document Type
Journal Article
Publication Date
2017-07-29
Subject Area
Files
Loading...
main.pdf
Adobe PDF, 3.53 MB
Embargo Expiration Date
Link to Full Text
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
Year of Medical School at Time of Visit
Sponsors
Dates of Travel
DOI
10.1016/j.ekir.2017.07.009
Permanent Link to this Item
PubMed ID
29270531
Other Identifiers
Notes
Funding and Acknowledgements
Corresponding Author
Related Resources
Related Resources
Repository Citation
Rights
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/).