Sorry, you need to enable JavaScript to visit this website.

Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity

TitleAutosomal recessive hereditary spastic paraplegia with thin corpus callosum: A novel mutation in the SPG11 gene and further evidence for genetic heterogeneity
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2009
AuthorsPippucci, T., Panza E., Pompilii E., Donadio V., Borreca A., Babalini C., Patrono Clarice, Zuntini R., Kawarai T., Bernardi G., Liguori R., Romeo G., Montagna P., Orlacchio A., and Seri M.
JournalEuropean Journal of Neurology
Volume16
Pagination121-126
ISSN13515101
Notes

cited By 12

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-57449117098&doi=10.1111%2fj.1468-1331.2008.02367.x&partnerID=40&md5=d6976a41a282db00c1ac13674be2f45d
DOI10.1111/j.1468-1331.2008.02367.x
Citation KeyPippucci2009121