Unraveling autism.
editorial · Level V
Where this comes from
- Record sourced from PubMed, PMID 18179879.
- Also identified by DOI 10.1016/j.ajhg.2007.12.003 and PMC identifier 2253980.
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Abstract
In this issue of AJHG, Alarcón et al.,(1) Arking et al.,(2) and Bakkaloglu et al.(3) identify a series of functional variants in the CNTNAP2 gene that unequivocally implicate this gene as causing Type 1 autism in the general population.
Medical subject headings
- Autistic Disorder