Autosomal dominant cerebellar ataxia, deafness and narcolepsy is caused by mutations of the DNMT1 gene.
1. |
Melberg A et al. (1995) Autosomal dominant cerebellar ataxia deafness and narcolepsy. |
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Winkelmann J et al. (2012) Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy. |
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Melberg A et al. (1999) Neuroimaging study in autosomal dominant cerebellar ataxia, deafness, and narcolepsy. |
4. |
OMIM.ORG article Omim 604121 |
5. |
Orphanet article Orphanet ID 314404 |