1. PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. Issue 5 (19th April 2017) Authors: Ozes, B.; Karagoz, N.; Schüle, R.; Rebelo, A.; Sobrido, M.‐J.; Harmuth, F.; Synofzik, M.; Pascual, S.I.P.; Colak, M.; Ciftci‐Kavaklioglu, B.; Kara, B.; Ordóñez‐Ugalde, A.; Quintáns, B.; Gonzalez, M.A.; Soysal, A.; Zuchner, S.; Battaloglu, E. Journal: Clinical genetics Issue: Volume 92:Issue 5(2017) Page Start: 534 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗