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Heterogeneous association between engrailed-2 and autism in the CPEA network

✍ Scribed by Camille W. Brune; Elena Korvatska; Kristina Allen-Brady; Edwin H. Cook Jr.; Geraldine Dawson; Bernie Devlin; Annette Estes; Meghann Hennelly; Susan L. Hyman; William M. McMahon; Jeffrey Munson; Patricia M. Rodier; Gerard D. Schellenberg; Christopher J. Stodgell; Hilary Coon


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
104 KB
Volume
147B
Category
Article
ISSN
1552-4841

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## Abstract A recent study by Persico et al. [2001: Mol Psychiatry 6:150–159] suggests alleles of a CGG polymorphism, just 5β€² of the reelin gene (__RELN__) initiator codon, confer liability for autism, especially alleles bearing 11 or more CGG repeats (long alleles). The association is consistent a

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## Abstract The Autism Genome Project (AGP) Consortium recently reported genome‐wide significant association between autism and an intronic single nucleotide polymorphism marker, rs4141463, within the MACROD2 gene. In the present study we attempted to replicate this finding using an independent cas