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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| Publication date | March 25, 2019 |
| Language | English |
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