Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

Author:

Campbell Daniel B.,Li Chun,Sutcliffe James S.,Persico Antonio M.,Levitt Pat

Publisher

Wiley

Subject

Genetics (clinical),Neurology (clinical),General Neuroscience

Reference31 articles.

1. Regulation and clinical significance of urokinase-receptor (u-PAR), an invasion-related molecule;Allgayer;Zeitschrift fur Gastroenterologie,2006

2. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations;Butler;Journal of Medical Genetics,2005

3. Disruption of cerebral cortex MET signaling in autism spectrum disorder;Campbell;Annals of Neurology,2007

4. A genetic variant that disrupts MET transcription is associated with autism;Campbell;Proceedings of the National Academy of Sciences of the United States of America,2006

5. Prevalence of autism spectrum disorders-autism and developmental disabilities monitoring network, 14 sites, United States, 2002;Centers for Disease Control and Prevention;Morbidity and Mortality Weekly Report: Surveillance Summaries,2007

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