Recurrent de novo mutations implicate novel genes underlying simplex autism risk

Saved in:
Bibliographic Details
Published inNature communications Vol. 5; no. 1; p. 5595
Main Authors O'Roak, B. J., Stessman, H. A., Boyle, E. A., Witherspoon, K. T., Martin, B., Lee, C., Vives, L., Baker, C., Hiatt, J. B., Nickerson, D. A., Bernier, R., Shendure, J., Eichler, E. E.
Format Journal Article
LanguageEnglish
Published 24.11.2014
Online AccessGet full text

Cover

More Information
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms6595