A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
Nature Genetics2006Vol. 38(5), pp. 525–527
Citations Over TimeTop 1% of 2006 papers
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
Related Papers
- → Fibrodysplasia ossificans progressiva (FOP): watch the great toes!(2010)38 cited
- → Rapid Progression of Heterotopic Ossification in Severe Variant of Fibrodysplasia Ossificans Progressiva with p.Arg258Gly in ACVR1: A Case Report and Review of Clinical Phenotypes(2022)4 cited
- → Fibrodysplasia Ossificans Progressiva: A Case Report(2013)3 cited
- Pseudomalignant heterotopic ossification.(1998)