SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia
Year: 2002
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng937
Authors: Heema Patel, Harold Cross, Christos Proukakis, Ruth Hershberger, Peer Bork, Francesca D. Ciccarelli, Michael A. Patton, Victor A. McKusick, Andrew H. Crosby
Institutions: University of London, St George's, University of London
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W1983685921
