Serine protease HtrA1 accumulates in corneal transforming growth factor beta induced protein (TGFBIp) amyloid deposits

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Specific mutations in the transforming growth factor beta induced (TGFBI) gene are associated with lattice corneal dystrophy (LCD) type 1 and its variants. In this study, we performed an in-depth proteomic analysis of human corneal amyloid deposits associated with the heterozygous A546D mutation in TGFBI
OriginalsprogEngelsk
TidsskriftMolecular Vision
Vol/bind19
Sider (fra-til)861-876
Antal sider16
ISSN1090-0535
StatusUdgivet - 12 apr. 2013

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