Novel apolipoprotein AII mutation associated renal amyloidosis and fibrillary/immunotactoid cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference9 articles.
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2. A new human hereditary amyloidosis: the result of a stop codon mutation in the apolipoprotein AII gene;Benson;Genomics,2001
3. Pathology of glomerular deposition disease;Joh;Pathol Int,2007
4. Renal diseases with organized deposits: an algorithmic approach to classification and clinicopathological diagnosis;Herrera;Arch Pathol Lab Med,2010
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Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The Roles of Fatty Acids and Apolipoproteins in the Kidneys;Metabolites;2022-05-20
2. Apolipoprotein genetic variants and hereditary amyloidosis;Current Opinion in Lipidology;2020-12-31
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