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	1.	[Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects]. [electronic resource] by Langouët, Maéva Mircsof, Dennis Rio, Marlène Amiel, Jeanne Brown, Steven A Colleaux, Laurence Producer: 20170718 In: Medecine sciences : M/S vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutation in TTI2 reveals a role for triple T complex in human brain development. [electronic resource] by Langouët, Maéva Saadi, Abdelkrim Rieunier, Guillaume Moutton, Sébastien Siquier-Pernet, Karine Fernet, Marie Nitschke, Patrick Munnich, Arnold Stern, Marc-Henri Chaouch, Malika Colleaux, Laurence Producer: 20140508 In: Human mutation vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons. [electronic resource] by Langouët, Maéva Glatt-Deeley, Heather R Chung, Michael S Dupont-Thibert, Clémence M Mathieux, Elodie Banda, Erin C Stoddard, Christopher E Crandall, Leann Lalande, Marc Producer: 20190107 In: Human molecular genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	An in vivo EGF receptor localization screen in C. elegans Identifies the Ezrin homolog ERM-1 as a temporal regulator of signaling. [electronic resource] by Haag, Andrea Gutierrez, Peter Bühler, Alessandra Walser, Michael Yang, Qiutan Langouët, Maeva Kradolfer, David Fröhli, Erika Herrmann, Christina J Hajnal, Alex Escobar-Restrepo, Juan M Producer: 20141125 In: PLoS genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy. [electronic resource] by Barcia, Giulia Fleming, Matthew R Deligniere, Aline Gazula, Valeswara-Rao Brown, Maile R Langouet, Maeva Chen, Haijun Kronengold, Jack Abhyankar, Avinash Cilio, Roberta Nitschke, Patrick Kaminska, Anna Boddaert, Nathalie Casanova, Jean-Laurent Desguerre, Isabelle Munnich, Arnold Dulac, Olivier Kaczmarek, Leonard K Colleaux, Laurence Nabbout, Rima Producer: 20130404 In: Nature genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects. [electronic resource] by Mircsof, Dennis Langouët, Maéva Rio, Marlène Moutton, Sébastien Siquier-Pernet, Karine Bole-Feysot, Christine Cagnard, Nicolas Nitschke, Patrick Gaspar, Ludmila Žnidarič, Matej Alibeu, Olivier Fritz, Ann-Kristina Wolfer, David P Schröter, Aileen Bosshard, Giovanna Rudin, Markus Koester, Christina Crestani, Florence Seebeck, Petra Boddaert, Nathalie Prescott, Katrina Hines, Rochelle Moss, Steven J Fritschy, Jean-Marc Munnich, Arnold Amiel, Jeanne Brown, Steven A Tyagarajan, Shiva K Colleaux, Laurence Producer: 20160314 In: Nature neuroscience vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)