Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype
Titel:
Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype
Auteur:
Morin, Matias Forst, Anna-Lena Pérez-Torre, Paula Jiménez-Escrig, Adriano Barca-Tierno, Verónica García-Galloway, Eva Warth, Richard Lopez-Sendón Moreno, Jose Luis Moreno-Pelayo, Miguel Angel