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)
Articolo
Data di Pubblicazione:
2019
Citazione:
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]
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
2708; Neurology (clinical); Psychiatry and Mental Health
Elenco autori:
A. Catania, L. Peverelli, S. Tabano, D. Ghezzi, C. Lamperti
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