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Functional modeling of the ACVR1 (R206H) mutation in FOP.
Groppe JC, Shore EM, Kaplan FS. Groppe JC, et al. Among authors: kaplan fs. Clin Orthop Relat Res. 2007 Sep;462:87-92. doi: 10.1097/BLO.0b013e318126c049. Clin Orthop Relat Res. 2007. PMID: 17572636
The Metamorphosis.
Kaplan FS. Kaplan FS. Clin Orthop Relat Res. 1998 Jan;(346):2-3. Clin Orthop Relat Res. 1998. PMID: 9577402 No abstract available.
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho TJ, Choi IH, Connor JM, Delai P, Glaser DL, LeMerrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS. Shore EM, et al. Among authors: kaplan fs. Nat Genet. 2006 May;38(5):525-7. doi: 10.1038/ng1783. Epub 2006 Apr 23. Nat Genet. 2006. PMID: 16642017
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