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Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutation
Mutations in exons 21 and 20 of the DMNT1 gene have been associated with two multisystem neurodegenerative diseases that involve central and peripheral nervous system ADCADN (Autosomal Dominant Cerebellar Ataxia with Deafness and Narcolepsy) and HSAN 1E (Hereditary Sensory and Autonomic Neuropathy I...
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| Pubblicato in: | J Clin Sleep Med |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Academy of Sleep Medicine
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7052993/ https://ncbi.nlm.nih.gov/pubmed/31957642 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5664/jcsm.8140 |
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