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) / A. Catania, L. Peverelli, S. Tabano, D. Ghezzi, C. Lamperti. - In: NEUROLOGICAL SCIENCES. - ISSN 1590-1874. - (2019). [Epub ahead of print] [10.1007/s10072-019-03859-7]

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)

L. Peverelli;S. Tabano;D. Ghezzi;C. Lamperti
2019

2708; Neurology (clinical); Psychiatry and Mental Health
Settore MED/26 - Neurologia
2019
25-mar-2019
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/642801
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