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)

Alessia Catania; Lorenzo Peverelli; Silvia Tabano; Daniele Ghezzi; Costanza Lamperti

doi: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)

Alessia Catania, Lorenzo Peverelli, Silvia Tabano, Daniele Ghezzi, Costanza Lamperti

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	1963-1966
Journal	Neurological Sciences
Volume	40
Issue number	9
DOIs	https://doi.org/10.1007/s10072-019-03859-7
Publication status	Published - Jan 1 2019

ASJC Scopus subject areas

Dermatology
Clinical Neurology
Psychiatry and Mental health

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10.1007/s10072-019-03859-7

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Catania, A., Peverelli, L., Tabano, S., Ghezzi, D., & Lamperti, C. (2019). 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). Neurological Sciences, 40(9), 1963-1966. https://doi.org/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). / Catania, Alessia; Peverelli, Lorenzo; Tabano, Silvia et al.

In: Neurological Sciences, Vol. 40, No. 9, 01.01.2019, p. 1963-1966.

Research output: Contribution to journal › Letter › peer-review

Catania, A, Peverelli, L, Tabano, S, Ghezzi, D & Lamperti, C 2019, '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)', Neurological Sciences, vol. 40, no. 9, pp. 1963-1966. https://doi.org/10.1007/s10072-019-03859-7

Catania A, Peverelli L, Tabano S, Ghezzi D, Lamperti C. 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). Neurological Sciences. 2019 Jan 1;40(9):1963-1966. https://doi.org/10.1007/s10072-019-03859-7

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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)

ASJC Scopus subject areas

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