A novel APOA1 mutation in a patient with renal amyloidosis: unveiling amyloid by next-generation sequencing

Amyloid. 2019 Dec;26(4):253-254. doi: 10.1080/13506129.2019.1660157. Epub 2019 Sep 4.

Authors

Francesca Cottini¹, Cherri Bott², Tibor Nadasdy², Sergey V Brodsky², Don Benson¹

Affiliations

¹ Division of Hematology, Department of Medicine, The Ohio State University , Columbus , OH , USA.
² Pathology Department, Ohio State University , Columbus , OH , USA.

PMID: 31482740
DOI: 10.1080/13506129.2019.1660157

No abstract available

Publication types

Case Reports

MeSH terms

Amyloidosis / genetics*
Amyloidosis / metabolism
Amyloidosis / pathology
Apolipoprotein A-I / genetics*
Apolipoprotein A-I / metabolism
Humans
Kidney Diseases / genetics*
Kidney Diseases / metabolism
Kidney Diseases / pathology
Male
Middle Aged
Mutation*

Substances

APOA1 protein, human
Apolipoprotein A-I