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cystatin C-associated amyloidosis

Tuesday 5 February 2008

Amyloidosis type 6 is caused by mutation in the gene encoding cystatin C (CST3) (MIM.604312), located on chromosome 20p11.2.

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  • Prion (a), cystatin C (b), transthyretin (TTR) amd amyloid fibril (...)