Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

by Wang, X., McCoy, P.A., Rodriguiz, R.M., Pan, Y., Je, H.S., Roberts, A.C., Kim, C.J., Berrios, J., Colvin, J.S., Bousquet-Moore, D., Lorenzo, I., Wu, G., Weinberg, R.J., Ehlers, M.D., Philpot, B.D., Beaudet, A.L., Wetsel, W.C., Jiang, Y.-H.
Published 2016

Recommendations for a nomenclature system for human gene mutations

by Antonarakis, S.E., Ashburner, M., Auerbach, A.D., Beaudet, A.L., Beckmann, J.S., Beutler, E., Cooper, D.N., Cotton, R.G.H., Den Dunnen, J.T., Desnick, R.J., Eng, C., Fasman, K.H., Goldman, D., Hayashi, K., Hutchinson, F., Kazazian Jr., H.H., Keen, J., King, M.-C., Lehvaslaiho, H., McAlpine, P.J., McKusick, V., Motulski, A.G., Povey, S., Schorderet, D.F., Scriver, C.R., Shows Jr., T.B., Supertifurga, A., Tay, A.H.N., Tsui, L.-C., Valle, D., Vihinen, M.
Published 2014