Autism, RCCX, C4b Deficiency & Synaptic Pruning
RCCX is a copy number variation (CNV) gene cluster located on chromosome 6. Variations of the RCCX genotype leads to an increased susceptibility to numerous diseases. Significant research links together one of the RCCX genes, C4b with autism, associated cell danger signaling, and problems related to neuronal, synaptic pruning. Last year I wrote an article