DOI:
10.1055/s-00000019
Fortschritte der Neurologie · Psychiatrie
LinksClose Window
References
Synofzik M et al.
Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype.
Neurobiol Aging 2012;
33 (12) 2949 e13-e17
We do not assume any responsibility for the contents of the web pages of other providers.