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adca-dn; dnmt1; hsan ie; cataplexy; narcolepsy; neurodegeneration; 14-3-3 proteins; adult; deafness; female; genetic predisposition to disease; hereditary sensory and autonomic neuropathies; humans; male; middle aged; mutation; narcolepsy; olivopontocerebellar atrophies; pedigree; phenotype (1) 1
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Journal Article
Journal Article
Sleep Medicine, ISSN 1389-9457, 2014, Volume 15, Issue 5, pp. 582 - 585
Journal Article
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Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 10/2015, Volume 23, Issue 11, pp. 1573 - 1580
Journal Article
Cerebellum (London, England), ISSN 1473-4222, 06/2019, pp. 1 - 6
Cerebellar ataxias are a clinically heterogeneous group of neurological disorders. Besides the cerebellum, several forms of hereditary ataxias or non-genetic... 
Cerebellum | Neurological diseases | Cochlea | Deafness | Vestibular system | Nystagmus
Journal Article
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