Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1
Titel:
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1
Auteur:
Moghadam, Keivan Kaveh Pizza, Fabio Tonon, Caterina Lodi, Raffaele Carelli, Valerio Poli, Francesca Franceschini, Christian Barboni, Piero Seri, Marco Ferrari, Simona La Morgia, Chiara Testa, Claudia Cornelio, Ferdinando Liguori, Rocco Winkelmann, Juliane Lin, Ling Mignot, Emmanuel Plazzi, Giuseppe