GRIN2A-related disorders: genotype and functional consequence predict phenotype

GRIN2A study group , Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, Katie F M Marwick, Gabrielle Rudolf, Julitta de Bellescize, Saskia Biskup, Eva H Brilstra, Oebele F Brouwer, Petra M C Callenbach, Julia Hentschel, Edouard Hirsch, Peter C Kind, Cyril Mignot, Konrad Platzer, Patrick Rump, Paul A Skehel, David J A Wyllie, Giles E HardinghamConny M A van Ravenswaaij-Arts, Gaetan Lesca, Johannes R Lemke

Deanery of Clinical Sciences
Edinburgh Neuroscience
Centre for Clinical Brain Sciences
Centre for Discovery Brain Sciences
Deanery of Biomedical Sciences
Edinburgh Imaging

Research output: Contribution to journal › Article › peer-review

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ECAT Fellowship for Katherine Marwick: Functional consequences of missense mutations in GRIN2A and GRIN2B associated withmental disorders
Hardingham, G.
UK-based charities
1/08/13 → 31/07/16
Project: Research

GRIN2A-related disorders: genotype and functional consequence predict phenotype

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ECAT Fellowship for Katherine Marwick: Functional consequences of missense mutations in GRIN2A and GRIN2B associated withmental disorders