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                                       Details for article 13 of 21 found articles
 
 
  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
 
 
Title: 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
Author: 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
Appeared in: Sleep medicine
Paging: Volume 15 (2014) nr. 5 pages 4 p.
Year: 2014
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 13 of 21 found articles
 
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