A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

著者: Eileen M. Shore, Meiqi Xu, George Feldman, David Fenstermacher, Tae‐Joon Cho, In Ho Choi, J. M. Connor, Patricia Delai, David L. Glaser, Martine LeMerrer, Rolf Morhart, John Rogers, Roger Smith, James T. Triffitt, Jon Andoni Urtizberea, Michael Zasloff, Matthew A. Brown, Frederick S. Kaplan - Nature Genetics 2006 被引用: 1,232