Schrewe, Heinrich Dept. of Developmental Genetics (Head: Bernhard G. Herrmann), Max Planck Institute for Molecular Genetics, Max Planck Society;
Schwaerzer.pdf (Verlagsversion), 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.
