SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia

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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

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