A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees

ConclusionsInclusion of subclinical phenotypes such as BAP should be more widely employed in genetic studies of ASD as a way of identifying inherited genetic variants for the disorder. Moreover, the results underscore the need for approaches to identifying genetic risk factors in extended pedigrees that are robust to high levels of inter/intrafamilial locus and allelic heterogeneity.
Source: Journal of Neurodevelopmental Disorders - Category: Neurology Source Type: research