(Q48114747)
Statements
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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. (English)
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Emmanuel Mignot
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Christian Franceschini
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Keivan Kaveh Moghadam
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Ferdinando Cornelio
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Piero Barboni
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Simona Ferrari
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Francesca Poli
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Ling Lin
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12 February 2014
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15
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5
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582-585
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