Schrewe, Heinrich Dept. of Developmental Genetics (Head: Bernhard G. Herrmann), Max Planck Institute for Molecular Genetics, Max Planck Society;
Schwaerzer.pdf (Publisher version), 2MB
Schwaerzer, G. K., Hiepen, C., Schrewe, H., Nickel, J., Ploeger, F., Sebald, W., et al. (2012). New insights into the molecular mechanism of multiple synostoses syndrome (SYNS): mutation within the GDF5 knuckle epitope causes noggin-resistance. Journal of Bone and Mineral Research, 27(2), 429-442. doi:10.1002/jbmr.532.