PedAM
Pediatric Disease Annotations & Medicines
| Disease | narcolepsy |
| Phenotype | C0007758|cerebellar ataxia |
| Sentences | 1 |
| PubMedID- 25669430 | As mutations in dnmt1 cause a rare dominant form of narcolepsy in association with deafness, cerebellar ataxia and dementia, we questioned whether the association with p2ry11 in sporadic narcolepsy could be secondary to linkage disequilibrium with dnmt1. |
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