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