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

Author(s):
Hor, H.; Bartesaghi, L.; Kutalik, Z.; Vicario, J.L.; Andres, C. de; Pfister, C.; Lammers, G.J.; Guex, N.; Chrast, R.; Tafti, M.; Peraita-Adrados, R.
Published
2011
Publication type
Article / Letter to editor
Date issued
2011-09-09
Language
English
Is part of
American Journal of Human Genetics (2011), Vol. 89, no. 3, p. 474-479
hdl
1887/102948
doi
10.1016/j.ajhg.2011.08.007