A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))

Nature Genetics 38, 525–527 (2006); published online 23 April; corrected after print 31 December 2006 In the version of this article initially published, several contributing authors were listed collectively under the name The FOP International Research Consortium. In order to facilitate the electronic citation of author contributions, the authors have chosen to delete the Consortium name and replace it with the names of the individual consortium authors in alphabetical order.