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

✍ Scribed by Hyun Hor; Luca Bartesaghi; Zoltán Kutalik; José L. Vicário; Clara de Andrés; Corinne Pfister; Gert J. Lammers; Nicolas Guex; Roman Chrast; Mehdi Tafti; Rosa Peraita-Adrados

Book ID: 119184362
Publisher: American Society of Human Genetics
Year: 2012
Tongue: English
Weight: 26 KB
Volume: 91
Category: Article
ISSN: 0002-9297
DOI: 10.1016/j.ajhg.2012.07.021

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