Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease.
| Autor: | Finsterer, J.1 fifigs1@yahoo.de, Wanschitz, J.2, Quasthoff, S.3, Iglseder, S.4, Löscher, W.2, Grisold, W.5 |
|---|---|
| Zdroj: | Acta Neurologica Scandinavica. Dec2017, Vol. 136 Issue 6, p558-569. 12p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
|