Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype

1. Morin, M.
2. Forst, A.-L.
3. Pérez-Torre, P.
4. Jiménez-Escrig, A.
5. Barca-Tierno, V.
6. García-Galloway, E.
7. Warth, R.
8. Lopez-Sendón Moreno, J.L.
9. Moreno-Pelayo, M.A.