Fig. 1From: A new synaptic player leading to autism risk: Met receptor tyrosine kinaseDiagram illustrating the three allelic variants of the gene encoding the MET receptor tyrosine kinase (MET) that have been associated with an increased risk for ASD in multiple independent studies. In addition, rare copy number variants (CNVs) that interrupt the MET gene have been associated with ASD. See reference list for citations noted in the figureBack to article page