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Publikováno v:
Molecular Imaging, Vol 16 (2017)
Amyloidosis is associated with a number of rare diseases and is characterized by the deposition, in abdominothoracic organs and peripheral nerves, of extracellular protein fibrils, which leads to dysfunction and severe morbidity. Effective clinical e
Externí odkaz:
https://doaj.org/article/14ecb53894044f948c61b7b1618f51d9
