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.
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| Description | scientific article |
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author: Fabio Pizza Emmanuel Mignot Marco Seri Giuseppe Plazzi Juliane Winkelmann Valerio Carelli Caterina Tonon Raffaele Lodi Rocco Liguori Chiara La Morgia Piero Barboni Christian Franceschini Keivan Kaveh Moghadam Simona Ferrari Ferdinando Cornelio Claudia Testa Francesca Poli |
| Publication date | February 12, 2014 |
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