De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia

  1. Van de Vondel, L.
  2. De Winter, J.
  3. Beijer, D.
  4. Coarelli, G.
  5. Wayand, M.
  6. Palvadeau, R.
  7. Pauly, M.G.
  8. Klein, K.
  9. Rautenberg, M.
  10. Guillot-Noël, L.
  11. Deconinck, T.
  12. Vural, A.
  13. Ertan, S.
  14. Dogu, O.
  15. Uysal, H.
  16. Brankovic, V.
  17. Herzog, R.
  18. Brice, A.
  19. Durr, A.
  20. Klebe, S.
  21. Stock, F.
  22. Bischoff, A.T.
  23. Rattay, T.W.
  24. Sobrido, M.-J.
  25. De Michele, G.
  26. De Jonghe, P.
  27. Klopstock, T.
  28. Lohmann, K.
  29. Zanni, G.
  30. Santorelli, F.M.
  31. Timmerman, V.
  32. Haack, T.B.
  33. Züchner, S.
  34. Schüle, R.
  35. Stevanin, G.
  36. Synofzik, M.
  37. Basak, A.N.
  38. Baets, J.
  39. Show all authors +
Journal:
Movement Disorders

ISSN: 1531-8257 0885-3185

Year of publication: 2022

Volume: 37

Issue: 6

Pages: 1175-1186

Type: Article

DOI: 10.1002/MDS.28959 GOOGLE SCHOLAR

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