Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia
Christel Depienne, Estelle Fedirko, Sylvie Forlani, Cécile Cazeneuve, Pascale Ribaï, Imed Feki, Chantal Tallaksen, Karine Nguyen, Bruno Stankoff, Merle Ruberg, Giovanni Stevanin, Alexandra Durr, Alexis Brice
Journal of Medical Genetics Apr 2007, 44 (4) 281-284; DOI: 10.1136/jmg.2006.046425