Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia

Item Type:Article
Title:SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia
Creators Name:Patel, H., Cross, H., Proukakis, C., Hershberger, R., Bork, P., Ciccarelli, F.D., Patton, M.A., McKusick, V.A. and Crosby, A.H.
Source:Nature Genetics
ISSN:1061-4036
Publisher:Nature Publishing Group
Volume:31
Page Range:347-348
Date:1 August 2002
Official Publication:https://doi.org/10.1038/ng937
PubMed:View item in PubMed

Repository Staff Only: item control page

Open Access
MDC Library