![](/img/cover-not-exists.png)
Seeking confidence in the diagnosis of systemic AL (Ig light-chain) amyloidosis: patients can have both monoclonal gammopathies and hereditary amyloid proteins
Comenzo, R. L.Volume:
107
Language:
english
Journal:
Blood
DOI:
10.1182/blood-2005-10-4148
Date:
May, 2006
File:
PDF, 84 KB
english, 2006