A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
Published Online: 2006-04-23
Journal: Nature Genetics•Publisher: Springer Science and Business Media LLC
Authors: David A Fenstermacher•David L Glaser•Eileen M Shore•Frederick S Kaplan•George J Feldman•In Ho Choi•J Andoni Urtizberea•J Michael Connor•James T Triffitt•John G Rogers•Martine LeMerrer•Matthew A Brown•Meiqi Xu•Michael Zasloff•Patricia Delai•Roger Smith•Rolf Morhart•Tae-Joon Cho
