Loading...

Recent advances in transthyretin amyloidosis therapy

Mutant (MT) forms of transthyretin (TTR) cause the most common type of autosomal-dominant hereditary systemic amyloidosis—familial amyloidotic polyneuropathy (FAP). Until 20 years ago, FAP was thought to be an endemic disease, but FAP is known to occur worldwide. To date, more than 130 mutations in...

Full description

Saved in:
Bibliographic Details
Main Authors: Ueda, Mitsuharu, Ando, Yukio
Format: Artigo
Language:Inglês
Published: BioMed Central 2014
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4165622/
https://ncbi.nlm.nih.gov/pubmed/25228988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2047-9158-3-19
Tags: Add Tag
No Tags, Be the first to tag this record!