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ACVR1<sup>R206H</sup> receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A.
Published in:
Science Translational Medicine, 2015, v. 7, n. 303, p. 1, doi. 10.1126/scitranslmed.aac4358
By:
- Hatsell, Sarah J.;
- Idone, Vincent;
- Alessi Wolken, Dana M.;
- Huang, Lily;
- Kim, Hyon J.;
- Lili Wang;
- Xialing Wen;
- Nannuru, Kalyan C.;
- Jimenez, Johanna;
- Liqin Xie;
- Das, Nanditha;
- Makhoul, Genevieve;
- Chernomorsky, Rostislav;
- D’Ambrosio, David;
- Corpina, Richard A.;
- Schoenherr, Christopher J.;
- Feeley, Kieran;
- Yu, Paul B.;
- Yancopoulos, George D.;
- Murphy, Andrew J.
Publication type:
Article