UMMS Affiliation

Proteomics and Mass Spectrometry Facility; Department of Biochemistry and Molecular Pharmacology

Publication Date

7-29-2017

Document Type

Article

Disciplines

Female Urogenital Diseases and Pregnancy Complications | Genetic Phenomena | Genetics and Genomics | Male Urogenital Diseases | Nephrology | Nutritional and Metabolic Diseases

Abstract

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

Rights and Permissions

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/).

DOI of Published Version

10.1016/j.ekir.2017.07.009

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

Journal/Book/Conference Title

Kidney international reports

Related Resources

Link to Article in PubMed

PubMed ID

29270531

Creative Commons License

Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.

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