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DNMT1-complex disorder caused by a novel mutation associated with an overlapping phenotype of autosomal-dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) and hereditary sensory neuropathy with dementia and hearing loss (HSN1E)

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Description scientific article published on 25 March 2019
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author: Alessia Catania 

Publication date March 25, 2019
Language English
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