Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease?
Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene
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Veröffentlicht in: | American journal of nephrology 2022-12, Vol.53 (8-9), p.624-627 |
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container_title | American journal of nephrology |
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creator | Allinovi, Marco Bergesio, Franco Cappelli, Francesco Chiappini, Maria Grazia Santostefano, Marisa Argirò, Alessia Catalucci, Tullio Parise, Alberto Zampieri, Mattia Perfetto, Federico |
description | Keywords: Transthyretin, Amyloidosis, Cardiorenal syndrome, Exome sequencing, TTR gene |
doi_str_mv | 10.1159/000526955 |
format | Article |
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issn | 0250-8095 1421-9670 |
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source | MEDLINE; Karger Journals |
subjects | Amyloid Neuropathies, Familial - complications Amyloid Neuropathies, Familial - genetics Amyloidosis Chronic kidney failure Complications and side effects Humans Mutation Perspective Polycystic Kidney, Autosomal Dominant - complications Polycystic Kidney, Autosomal Dominant - genetics Renal Insufficiency, Chronic - complications Renal Insufficiency, Chronic - genetics Risk factors |
title | Is Hereditary Transthyretin Amyloidosis the Third Leading Cause of Monogenic Chronic Kidney Disease, Only Behind ADPKD and Alport Disease? |
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