Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleSPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.AuthorsPatel H; Cross H; Proukakis C; Hershberger R; Bork P; Ciccarelli FD; Patton MA; McKusick VA; Crosby AHPublicationNature genetics, 2002, Vol 31, Issue 4, p347ISSN1061-4036Publication typearticleDOI10.1038/ng937