HuGE Literature Finder
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Recurrent de novo mutations implicate novel genes underlying simplex autism risk. Nature communications 2014 5 5595. 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 |
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- Page last updated:Mar 16, 2023
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