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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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| 出版年: | J Clin Sleep Med |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Academy of Sleep Medicine
2020
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| 主題: | |
| オンライン･アクセス: | 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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