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Autosomal dominant hereditary spastic paraplegia: DHPLC-based mutation analysis of SPG4 reveals eleven novel mutations.
Clarice Patrono, Valentina Scarano, Federica Cricchi, Mariarosa A B Melone, Maria Chiriaco, Alessandro Napolitano, Alessandro Malandrini, Giuseppe De Michele, Lucia Petrozzi, Carlo Giraldi, Lucio Santoro, Serena Servidei, Carlo Casali, Alessandro Filla, Filippo M. Santorelli
Research output: Contribution to journal › Article › peer-review