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Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.

TitleAutosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2005
AuthorsPatrono, Clarice, Scarano V., Cricchi F., Melone M.A., Chiriaco M., Napolitano A., Malandrini A., De Michele G., Petrozzi L., Giraldi C., Santoro L., Servidei S., Casali C., Filla A., and Santorelli F.M.
JournalHuman mutation
Volume25
Pagination506
ISSN10981004
Notes

cited By 40

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-28544451984&doi=10.1002%2fhumu.9340&partnerID=40&md5=f880ff80c63f444469bd9d458ece373b
DOI10.1002/humu.9340
Citation KeyPatrono2005506