Associated Papers
Autism patient-derived SHANK2BY29X mutation affects the development of ALDH1A1 negative dopamine neuron.
Lai W et al.
Molecular Psychiatry, 2024
Distinct Phenotypes of Shank2 Mouse Models Reflect Neuropsychiatric Spectrum Disorders of Human Patients With SHANK2 Variants.
Eltokhi A et al.
Frontiers in Molecular Neuroscience, 2018
30072871 (PubMed )
Supplement: Table_1.pdf
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Leblond CS et al.
Plos Genetics, 2012
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