| Issue |
Med Sci (Paris)
Volume 32, Number 6-7, Juin–Juillet 2016
|
|
|---|---|---|
| Page(s) | 571 - 573 | |
| Section | Nouvelles | |
| DOI | https://doi.org/10.1051/medsci/20163206015 | |
| Published online | 12 July 2016 | |
Les mutations du gène NONO sont responsables d’un nouveau syndrome de déficience intellectuelle lié au dysfonctionnement des synapses inhibitrices
Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects
1
Inserm UMR 1163, laboratoire bases moléculaires et pathophysiologiques des désordres cognitifs, université Paris Descartes– Sorbonne Paris Cité, institut Imagine, hôpital Necker-Enfants Malades, 24, boulevard du Montparnasse, 75015 Paris, France
2
Chronobiology and Sleep Research Group, Neuromorphology Group, Institute of Pharmacology, Inserm UMR 1163, Hôpital Necker Enfants Malades, 149, rue de Sèvres, 75015 Paris, France
3
Neuromorphology Group, Institute of Pharmacology and Toxicology, University of Zurich, 190 Winterthurerstrasse, 8057 Zurich, Suisse
*
maeva.langouet@gmail.com
**
laurence.colleaux@inserm.fr
Cet article ne possède pas de résumé.
© 2016 médecine/sciences – Inserm
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.
