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pro vyhledávání: '"genetics [Cerebral Amyloid Angiopathy, Familial]"'
Autor:
Birkir Thor Bragason, Stephan A. Kaeser, Elias Olafsson, Helgi J Isaksson, Angelos Skodras, Astridur Palsdottir, Asbjorg Osk Snorradottir
Publikováno v:
Brain research 1622, 149-162 (2015). doi:10.1016/j.brainres.2015.06.019
Hereditary Cystatin C Amyloid Angiopathy (HCCAA) is an amyloid disorder in Icelandic families caused by an autosomal dominant mutation in the cystatin C gene. Mutant cystatin C forms amyloid deposits in brain arteries and arterioles which are associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d10992ed6449c64fe8ff8d5d009501b
