De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Titel:
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Auteur:
Küry, Sébastien van Woerden, Geeske M. Besnard, Thomas Proietti Onori, Martina Latypova, Xénia Towne, Meghan C. Cho, Megan T. Prescott, Trine E. Ploeg, Melissa A. Sanders, Stephan Stessman, Holly A.F. Pujol, Aurora Distel, Ben Robak, Laurie A. Bernstein, Jonathan A. Denommé-Pichon, Anne-Sophie Lesca, Gaëtan Sellars, Elizabeth A. Berg, Jonathan Carré, Wilfrid Busk, Øyvind Løvold van Bon, Bregje W.M. Waugh, Jeff L. Deardorff, Matthew Hoganson, George E. Bosanko, Katherine B. Johnson, Diana S. Dabir, Tabib Holla, Øystein Lunde Sarkar, Ajoy Tveten, Kristian de Bellescize, Julitta Braathen, Geir J. Terhal, Paulien A. Grange, Dorothy K. van Haeringen, Arie Lam, Christina Mirzaa, Ghayda Burton, Jennifer Bhoj, Elizabeth J. Douglas, Jessica Santani, Avni B. Nesbitt, Addie I. Helbig, Katherine L. Andrews, Marisa V. Begtrup, Amber Tang, Sha van Gassen, Koen L.I. Juusola, Jane Foss, Kimberly Enns, Gregory M. Moog, Ute Hinderhofer, Katrin Paramasivam, Nagarajan Lincoln, Sharyn Kusako, Brandon H. Lindenbaum, Pierre Charpentier, Eric Nowak, Catherine B. Cherot, Elouan Simonet, Thomas Ruivenkamp, Claudia A.L. Hahn, Sihoun Brownstein, Catherine A. Xia, Fan Schmitt, Sébastien Deb, Wallid Bonneau, Dominique Nizon, Mathilde Quinquis, Delphine Chelly, Jamel Rudolf, Gabrielle Sanlaville, Damien Parent, Philippe Gilbert-Dussardier, Brigitte Toutain, Annick Sutton, Vernon R. Thies, Jenny Peart-Vissers, Lisenka E.L.M. Boisseau, Pierre Vincent, Marie Grabrucker, Andreas M. Dubourg, Christèle Tan, Wen-Hann Verbeek, Nienke E. Granzow, Martin Santen, Gijs W.E. Shendure, Jay Isidor, Bertrand Pasquier, Laurent Redon, Richard Yang, Yaping State, Matthew W. Kleefstra, Tjitske Cogné, Benjamin Petrovski, Slavé Retterer, Kyle Eichler, Evan E. Rosenfeld, Jill A. Agrawal, Pankaj B. Bézieau, Stéphane Odent, Sylvie Elgersma, Ype Mercier, Sandra