Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emerging
- PMID: 18413565
- DOI: 10.1212/01.wnl.0000310433.12618.e4
Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emerging
Comment on
-
SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia.Neurology. 2008 Apr 15;70(16 Pt 2):1384-9. doi: 10.1212/01.wnl.0000294327.66106.3d. Epub 2008 Mar 12. Neurology. 2008. PMID: 18337587 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources