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Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5392243
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https://collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5392243
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Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects
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United States: Nature Publishing Group
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English
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The DDD Study
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
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5392243
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https://collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5392243
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