A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy

Narcolepsy is a rare sleep disorder characterized by excessive daytime sleepiness and cataplexy. Familial narcolepsy accounts for less than 10% of all narcolepsy cases. However, documented multiplex families are very rare and causative mutations have not been identified to date. To identify a causat...

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Autors principals: Hor, Hyun, Bartesaghi, Luca, Kutalik, Zoltán, Vicário, José L., de Andrés, Clara, Pfister, Corinne, Lammers, Gert J., Guex, Nicolas, Chrast, Roman, Tafti, Mehdi, Peraita-Adrados, Rosa
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3169816/
https://ncbi.nlm.nih.gov/pubmed/21907016
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2011.08.007
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