Prokaeva, TatianaAkar, HarunSpencer, BrianHavasi, AndreaCui, HailiO'Hara, Carl J.Gursky, OlgaLeszyk, John D.Steffen, MartinBrowning, SabrinaRosenberg, AllisonConnors, Lawreen H.2022-08-232022-08-232017-07-292018-03-27<p>Kidney Int Rep. 2017 Jul 29;2(6):1223-1232. doi: 10.1016/j.ekir.2017.07.009. eCollection 2017 Nov. <a href="https://doi.org/10.1016/j.ekir.2017.07.009">Link to article on publisher's site</a></p>2468-0249 (Linking)10.1016/j.ekir.2017.07.00929270531https://hdl.handle.net/20.500.14038/40514Here, we report a family with renal amyloidosis associated with a novel stop codon mutation in APOA2 and the apoA-II variant, 78Leuext21.en-USCopyright 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/).http://creativecommons.org/licenses/by-nc-nd/4.0/Female Urogenital Diseases and Pregnancy ComplicationsGenetic PhenomenaGenetics and GenomicsMale Urogenital DiseasesNephrologyNutritional and Metabolic DiseasesHereditary Renal Amyloidosis Associated With a Novel Apolipoprotein A-II VariantJournal Articlehttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4328&context=oapubs&unstamped=1https://escholarship.umassmed.edu/oapubs/331711856467oapubs/3317