Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype
- Morin, M.
- Forst, A.-L.
- Pérez-Torre, P.
- Jiménez-Escrig, A.
- Barca-Tierno, V.
- García-Galloway, E.
- Warth, R.
- Lopez-Sendón Moreno, J.L.
- Moreno-Pelayo, M.A.
ISSN: 1364-6753, 1364-6745
Argitalpen urtea: 2020
Alea: 21
Zenbakia: 2
Orrialdeak: 135-143
Mota: Artikulua