Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva. by Virdi, A, Shore, E, Oreffo, R, Li, M, Connor, J, Smith, R, Kaplan, F, Triffitt, J

Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527)) by Shore, E, Xu, M, Feldman, G, Fenstermacher, D, Cho, T, Choi, I, Connor, J, Delai, P, Glaser, D, LeMerrer, M, Morhart, R, Rogers, J, Smith, R, Triffitt, J, Urtizberea, J, Zasloff, M, Brown, M, Kaplan, F

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. by Shore, E, Xu, M, Feldman, G, Fenstermacher, D, Cho, T, Choi, I, Connor, J, Delai, P, Glaser, D, LeMerrer, M, Morhart, R, Rogers, J, Smith, R, Triffitt, J, Urtizberea, J, Zasloff, M, Brown, M, Kaplan, F

Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al. by Kaplan, F, Xu, M, Feldman, G, Brown, M, Cho, T, Choi, I, Connor, J, Delai, P, Economides, A, Glaser, D, Groppe, J, Katagiri, T, Le Merrer, M, Morhart, R, Ravazzolo, R, Rogers, J, Smith, R, Triffitt, J, Urtizberea, J, Zasloff, M, Shore, E