Evaluation of the therapeutic potential of a CNP analog in a Fgfr3 mouse model recapitulating achondroplasia.
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A. Munnich | S. Bunting | C. O’Neill | F. Di Rocco | L. Tsuruda | Sherry Bullens | N. Kaci | C. Benoist-Lasselin | L. Legeai-Mallet | S. Bell | Todd Oppeneer | D. Wendt | F. Lorget | Jeff W. Peng | E. Mugniery | S. Bullens