Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans von Wu, Ye, Arai, Amy C, Rumbaugh, Gavin, Srivastava, Anand K, Turner, Gillian, Hayashi, Takashi, Suzuki, Erika, Jiang, Yuwu, Zhang, Lilei, Rodriguez, Jayson, Boyle, Jackie, Tarpey, Patrick, Raymond, F. Lucy, Nevelsteen, Joke, Froyen, Guy, Stratton, Mike, Futreal, Andy, Gecz, Jozef, Stevenson, Roger, Schwartz, Charles E, Valle, David, Huganir, Richard L, Wang, Tao

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Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disability von Vanmarsenille, Lieselot, Verbeeck, Jelle, Belet, Stefanie, Roebroek, Anton J, Van de Putte, Tom, Nevelsteen, Joke, Callaerts-Vegh, Zsuzsanna, D'Hooge, Rudi, Marynen, Peter, Froyen, Guy

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Generation and Characterization of an Nxf7 Knockout Mouse to Study NXF5 Deficiency in a Patient with Intellectual Disability von Vanmarsenille, Lieselot, Verbeeck, Jelle, Belet, Stefanie, Roebroek, Anton, Van de Putte, Tom, Nevelsteen, Joke, Callaerts-Vegh, Zsuzsanna, D'Hooge, Rudi, Marynen, Peter, Froyen, Guy

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Detection and validation of copy number variation in X-linked mental retardation von Bauters, Marijke, Weuts, An, Vandewalle, Joke, Nevelsteen, Joke, Marynen, Peter, Van Esch, Hilde, Froyen, Guido

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Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans von Wu, Ye, Arai, Amy C, Rumbaugh, Gavin, Srivastava, Anand K, Turner, Gillian, Hayashi, Takashi, Suzuki, Erika, Jiang, Yuwu, Zhang, Lilei, Rodriguez, Jayson, Boyle, Jackie, Tarpey, Patrick, Raymond, F. Lucy, Nevelsteen, Joke, Froyen, Guido, Stratton, Mike, Futreal, Andy, Gecz, Jozef, Stevenson, Roger, Schwartz, Charles E, Valle, David, Huganir, Richard L, Wang, Tao

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