Wird geladen...
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...
Gespeichert in:
| Veröffentlicht in: | J Clin Sleep Med |
|---|---|
| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Academy of Sleep Medicine
2020
|
| Schlagworte: | |
| Online Zugang: | 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 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|