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. 2011 Jan 7;88(1):121. doi: 10.1016/j.ajhg.2010.12.005

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

Daniel Moreno-De-Luca ∗; SGENE Consortium, Jennifer G Mulle; Simons Simplex Collection Genetics Consortium, Erin B Kaminsky, Stephan J Sanders; GeneSTAR, Scott M Myers, Margaret P Adam, Amy T Pakula, Nancy J Eisenhauer, Kim Uhas, LuAnn Weik, Lisa Guy, Melanie E Care, Chantal F Morel, Charlotte Boni, Bonnie Anne Salbert, Ashadeep Chandrareddy, Laurie A Demmer, Eva WC Chow, Urvashi Surti, Swaroop Aradhya, Diane L Pickering, Denae M Golden, Warren G Sanger, Emily Aston, Arthur R Brothman, Troy J Gliem, Erik C Thorland, Todd Ackley, Ram Iyer, Shuwen Huang, John C Barber, John A Crolla, Stephen T Warren, Christa L Martin, David H Ledbetter ∗∗
PMCID: PMC3014368

(The American Journal of Human Genetics 87, 618–630; November 12, 2010)

In the original version of this article, one grant was left out of the Acknowledgments. The corrected version of the sentence appears here:

Acknowledgments

This work was funded in part by NIH grants MH074090 (D.H.L. and C.L.M.), HD064525 (D.H.L. and C.L.M.), MH081754 (CLM), MH080583 (J.G.M.), MH080129 (S.T.W.), and MH071425 (K. Stefansson).

Contributor Information

Daniel Moreno-De-Luca, Email: daniel.morenodeluca@emory.edu.

David H. Ledbetter, Email: david.ledbetter@emory.edu.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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