| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3177776 | Sleep Medicine | 2007 | 5 Pages |
Abstract
This result supports existing evidence which indicates that mutations of the prepro-orexin gene are rare and that the genetic contribution to the aetiology of human narcolepsy is likely to be complex.
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Authors
Timothy G. Quinnell, I. Sadaf Farooqi, Ian E. Smith, John M. Shneerson,