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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E. Mignot | F. Poli | G. Plazzi | P. Barboni | R. Lodi | J. Winkelmann | C. La Morgia | C. Testa | C. Tonon | F. Pizza | F. Cornelio | Ling Lin | V. Carelli | R. Liguori | C. Franceschini | M. Seri | S. Ferrari | K. K. Moghadam
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