Hofmeister, W., Nilsson, D., Topa, A., Anderlid, B.M., Darki, F., Matsson, H., Tapia Páez, I., Klingberg, T., Samuelsson, L., Wirta, V., Vezzi, F., Kere, J., Nordenskjöld, M., Syk Lundberg, E., Lindstrand, A. (2015) CTNND2-a candidate gene for reading problems and mild intellectual disability. Journal of Medical Genetics. 52(2):111-22

Hofmeister, W., Nilsson, D., Topa, A., Anderlid, B.M., Darki, F., Matsson, H., Tapia Páez, I., Klingberg, T., Samuelsson, L., Wirta, V., Vezzi, F., Kere, J., Nordenskjöld, M., Syk Lundberg, E., Lindstrand, A. (2015) CTNND2-a candidate gene for reading problems and mild intellectual disability. Journal of Medical Genetics. 52(2):111-22