De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females

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@inproceedings{Popp2015DeNM, title={De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females}, author={Bernt Popp and Svein Isungset St\ove and Sabine U Endele and Line M. Myklebust and Juliane Hoyer and Heinrich Sticht and Silvia Azzarello-Burri and Anita Rauch and Thomas Arnesen and Andr{\'e} Reis}, booktitle={European journal of human genetics : EJHG}, year={2015} }