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Paper Details

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
PLoS Genet
306
2012
15q11-q13, ASD, Autism, Autism spectrum disorders, CHRNA7, CYFIP1, SHANK2, SHANK2 deletion, SHANK2 deletions, SHANK2 mutations, amino acids, autism, autism spectrum disorders, neurodevelopmental disorders, neuronal cell cultures, neuropsychiatric disorders, nicotinic receptor CHRNA7, patient, patients, putative modifier genes, synaptic gene

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Release 1.2