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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)

Crossref DOI link: https://doi.org/10.1007/s10072-019-03859-7

Published Online: 2019-03-25

Published Print: 2019-09

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Catania, Alessia https://orcid.org/0000-0001-9948-5906
Peverelli, Lorenzo

Tabano, Silvia

Ghezzi, Daniele

Lamperti, Costanza
Funding

Funding for this research was provided by:

Fondazione Pierfranco e Luisa Mariani (CM23)

Fondazione Telethon (GGP15041)

H2020 European Research Council (GENOMIT)
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Article History

Received: 18 January 2019

Accepted: 19 March 2019

First Online: 25 March 2019

Compliance with ethical standards

:

: The authors declare that they have no conflict of interest.

: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

: Informed consent was obtained from all individual participants included in the study.

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