Communicated by William S. Oetting
A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder†
Article first published online: 12 NOV 2012
© 2012 Wiley Periodicals, Inc.
Volume 33, Issue 12, pages 1639–1646, December 2012
How to Cite
Puffenberger, E. G., Jinks, R. N., Wang, H., Xin, B., Fiorentini, C., Sherman, E. A., Degrazio, D., Shaw, C., Sougnez, C., Cibulskis, K., Gabriel, S., Kelley, R. I., Morton, D. H. and Strauss, K. A. (2012), A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder. Hum. Mutat., 33: 1639–1646. doi: 10.1002/humu.22237
- Issue published online: 12 NOV 2012
- Article first published online: 12 NOV 2012
- Accepted manuscript online: 15 OCT 2012 04:35AM EST
- Manuscript Accepted: 10 OCT 2012
- Manuscript Received: 27 APR 2012
- Contract grant sponsors: National Human Genome Research Institute of the National Institutes of Health (NIH) (U54 HG003067); Howard Hughes Medical Institute's Undergraduate Science Education Program (52006294).
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