Renal ApoA-1 Amyloidosis with Glu34Lys Mutation and Intra-amyloid Lipid Accumulation

Apolipoprotein A-1 (ApoA-1) amyloidosis occurs as a nonhereditary condition in atherosclerotic plaques, but it can also manifest as a hereditary disorder caused by mutations of the APOA1 gene. Hereditary ApoA-1 amyloidosis presents with diverse organ involvement based on the position of the mutation...

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Detaylı Bibliyografya
Yayımlandı:J Am Soc Nephrol
Asıl Yazarlar: Andeen, Nicole K., Lam, Daniel Y., de Boer, Ian H., Nicosia, Roberto F.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Nephrology 2014
Konular:
Up Front Matters
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4243342/
https://ncbi.nlm.nih.gov/pubmed/24925720
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2013060651
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