Litcius/Paper detail

Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia

Anna Alkelai, Shahar Shohat, Lior Greenbaum, Tanya Schechter, Benjamin Draiman, Eti Chitrit-Raveh, Shlomit Rienstein, Neha Dagaonkar, Daniel Hughes, Vimla S. Aggarwal, Erin L. Heinzen, Sagiv Shifman, David B. Goldstein, Yoav Kohn

2020Journal of Human Genetics27 citationsDOI

Topics & Concepts

PhenotypeLoss functionSchizophrenia (object-oriented programming)GeneticsBiologyMutationNeurodevelopmental disorderEpilepsyGenetic heterogeneityMedicineNeurosciencePsychiatryGeneGenetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology ResearchReceptor Mechanisms and Signaling
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia | Litcius