Researchers Find De Novo Autism Mutations Using Exome Sequencing | GenomeWeb Daily News |

The mutations found by exome sequencing were in the FOXP1 (Forkhead box transcription factor), GRIN2B (NMDA receptror) , SCN1(Sodium channel) , and LAMC3 ( a laminin extracellular matrix glycoprotein) genes.


Risk factors: Autism risk factors and KEGG pathways :
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