| Literature DB >> 18590993 |
Eileen M Shore1, Frederick S Kaplan.
Abstract
Fibrodysplasia ossificans progressiva (FOP) is a rare human genetic disorder of extensive and debilitating extra-skeletal bone formation. While the challenges of investigating a rare condition are many, the potential benefits are also great - not only for the specific disease under investigation, but also for the unique perspective on how cells normally function and the mechanisms that underlie more common disorders. This review will illustrate some of the many insights that we have gained by studying FOP.Entities:
Mesh:
Year: 2008 PMID: 18590993 PMCID: PMC2601573 DOI: 10.1016/j.bone.2008.05.013
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398