Encontrado 1 documento, a visualizar página 1 de 1

Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the d...

Abstract Autism is a neurodevelopmental disorder of unclear etiology. The consistent finding of platelet hyperserotonemia in a proportion of patients and its heritability within affected families suggest that genes involved in the serotonin system play a role in this disorder. The role in autism etiology of seven candidate genes in the serotonin metabolic and neurotransmission pathways and mapping to autism li...