APA

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. (20150730). Recurrent de novo mutations implicate novel genes underlying simplex autism risk. : Nature communications.

Chicago

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 and Eichler E E. 20150730. Recurrent de novo mutations implicate novel genes underlying simplex autism risk. : Nature communications.

Harvard

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. and Eichler E. E. (20150730). Recurrent de novo mutations implicate novel genes underlying simplex autism risk. : Nature communications.

MLA

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 and Eichler E E. Recurrent de novo mutations implicate novel genes underlying simplex autism risk. : Nature communications. 20150730.