| Literature DB >> 28449898 |
Thomas Megelin1, Benjamin Thomas2, Xavier Ferrer3, Imad Ghorayeb4.
Abstract
Entities:
Keywords: Agrypnia excitata; D178N mutation; Fatal familial insomnia; Myoclonus; PRNP gene; Prion disease
Mesh:
Substances:
Year: 2017 PMID: 28449898 DOI: 10.1016/j.sleep.2017.02.015
Source DB: PubMed Journal: Sleep Med ISSN: 1389-9457 Impact factor: 3.492