Hirata, H., Nanda, I., van Riesen, A., McMichael, G., Hu, H., Hambrock, M., Papon, M.A., Fischer, U., Marouillat, S., Ding, C., Alirol, S., Bienek, M., Preisler-Adams, S., Grimme, A., Seelow, D., Webster, R., Haan, E., Maclennan, A., Stenzel, W., Yap, T.Y., Gardner, A., Nguyen, L.S., Shaw, M., Lebrun, N., Haas, S.A., Kress, W., Haaf, T., Schellenberger, E., Chelly, J., Viot, G., Shaffer, L.G., Rosenfeld, J.A., Kramer, N., Falk, R., El-Khechen, D., Escobar, L.F., Hennekam, R., Wieacker, P., Hübner, C., Ropers, H.H., Gecz, J., Schuelke, M., Laumonnier, F., and Kalscheuer, V.M. (2013) ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity. American journal of human genetics. 92(5):681-695

Hirata, H., Nanda, I., van Riesen, A., McMichael, G., Hu, H., Hambrock, M., Papon, M.A., Fischer, U., Marouillat, S., Ding, C., Alirol, S., Bienek, M., Preisler-Adams, S., Grimme, A., Seelow, D., Webster, R., Haan, E., Maclennan, A., Stenzel, W., Yap, T.Y., Gardner, A., Nguyen, L.S., Shaw, M., Lebrun, N., Haas, S.A., Kress, W., Haaf, T., Schellenberger, E., Chelly, J., Viot, G., Shaffer, L.G., Rosenfeld, J.A., Kramer, N., Falk, R., El-Khechen, D., Escobar, L.F., Hennekam, R., Wieacker, P., Hübner, C., Ropers, H.H., Gecz, J., Schuelke, M., Laumonnier, F., and Kalscheuer, V.M. (2013) ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity. American journal of human genetics. 92(5):681-695