Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2
J. Clin. Invest. Petra Seemann, et al. 115:2373 doi:10.1172/JCI25118 [Go to this article.]

Table 1
Binding affinities of WT GDF5 and mutant GDF5 to BMPR1A, BMPR1B, and NOG as determined by Biosensor interaction analysis