Show simple item record

dc.contributor.authorProkaeva, Tatiana
dc.contributor.authorAkar, Harun
dc.contributor.authorSpencer, Brian
dc.contributor.authorHavasi, Andrea
dc.contributor.authorCui, Haili
dc.contributor.authorO'Hara, Carl J.
dc.contributor.authorGursky, Olga
dc.contributor.authorLeszyk, John D.
dc.contributor.authorSteffen, Martin
dc.contributor.authorBrowning, Sabrina
dc.contributor.authorRosenberg, Allison
dc.contributor.authorConnors, Lawreen H.
dc.date2022-08-11T08:09:49.000
dc.date.accessioned2022-08-23T16:44:30Z
dc.date.available2022-08-23T16:44:30Z
dc.date.issued2017-07-29
dc.date.submitted2018-03-27
dc.identifier.citation<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>
dc.identifier.issn2468-0249 (Linking)
dc.identifier.doi10.1016/j.ekir.2017.07.009
dc.identifier.pmid29270531
dc.identifier.urihttp://hdl.handle.net/20.500.14038/40514
dc.description.abstractHere, we report a family with renal amyloidosis associated with a novel stop codon mutation in APOA2 and the apoA-II variant, 78Leuext21.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29270531&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733886/
dc.rightsCopyright 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/).
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectFemale Urogenital Diseases and Pregnancy Complications
dc.subjectGenetic Phenomena
dc.subjectGenetics and Genomics
dc.subjectMale Urogenital Diseases
dc.subjectNephrology
dc.subjectNutritional and Metabolic Diseases
dc.titleHereditary Renal Amyloidosis Associated With a Novel Apolipoprotein A-II Variant
dc.typeJournal Article
dc.source.journaltitleKidney international reports
dc.source.volume2
dc.source.issue6
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4328&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3317
dc.identifier.contextkey11856467
refterms.dateFOA2022-08-23T16:44:30Z
html.description.abstract<p>Here, we report a family with renal amyloidosis associated with a novel stop codon mutation in <em>APOA2</em> and the apoA-II variant, 78Leuext21.</p>
dc.identifier.submissionpathoapubs/3317
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProteomics and Mass Spectrometry Facility
dc.source.pages1223-1232


Files in this item

Thumbnail
Name:
Publisher version
Thumbnail
Name:
main.pdf
Size:
3.525Mb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

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/).
Except where otherwise noted, this item's license is described as 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/).