- Title
- A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population
- Creators - without role
- Maïté Amy - Imaging, Brain & NeuropsychiatryOliver StaehlinFrédérique René - Mécanismes Centraux et Périphériques de la NeurodégénérescenceHélène Blasco - Imaging, Brain & NeuropsychiatrySylviane Marouillat - Imaging, Brain & NeuropsychiatryHussein Daoud - Imaging, Brain & NeuropsychiatryPatrick Vourc'H - Imaging, Brain & NeuropsychiatryPaul H. GordonWilliam Camu - Université de MontpellierPhilippe Corcia - Centre Hospitalier Régional Universitaire de ToursJean-Philippe Loeffler - Mécanismes Centraux et Périphériques de la NeurodégénérescenceMiklós Palkovits - Semmelweis UniversityWolfgang H. SommerChristian R. Andres - Imaging, Brain & Neuropsychiatry
- Publication Details
- Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol.16(7-8), pp.490--496
- Identifiers
- 9933908809311
- Academic Unit
- Université de Montpellier
- Language
- English
- Resource Type
- Journal article
- Local Fields
- hal-01985793
Journal article
A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol.16(7-8), pp.490--496
2015
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