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

By E. Shore, Meiqi Xu, G. Feldman, David A. Fenstermacher, T. Cho, I. Choi, J. Connor, P. Delai, D. Glaser, M. Lemerrer and 8 more. Nature Genetics, 2006

1,169 citations recorded by the source corpus.

Subfields: Molecular Biology, Pulmonary and Respiratory Medicine, Rheumatology

View Paper: https://www.semanticscholar.org/paper/205d6d4a5837ea844f8b15e1063ee30a32bbf854

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In Molecular Biology

  1. Randall T. Peterson

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