PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

1. Ozes, B.
2. Karagoz, N.
3. Schüle, R.
4. Rebelo, A.
5. Sobrido, M.-J.
6. Harmuth, F.
7. Synofzik, M.
8. Pascual, S.I.P.
9. Colak, M.
10. Ciftci-Kavaklioglu, B.
11. Kara, B.
12. Ordóñez-Ugalde, A.
13. Quintáns, B.
14. Gonzalez, M.A.
15. Soysal, A.
16. Zuchner, S.
17. Battaloglu, E.