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Fibrodysplasia ossificans progressiva: Middle-age onset of heterotopic ossification from a unique missense mutation (c.974G > C, p.G325A) inACVR1

  • Published:2012-02-21 Issue:3 Volume:27 Page:729-737
  • ISSN:0884-0431
  • Container-title:Journal of Bone and Mineral Research
  • language:en
  • Short-container-title:J Bone Miner Res

Author:

Whyte Michael P,Wenkert Deborah,Demertzis Jennifer L,DiCarlo Edward F,Westenberg Erica,Mumm Steven

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference41 articles.

1. Online Mendelian Inheritance in Man (OMIM) [Internet] http://www.ncbi.nlm.nih.gov/omim/

2. Fibrodysplasia ossificans progressiva;Kaplan;Best Pract Res Clin Rheumatol.,2008

3. Osteochondral diseases and fibrodysplasia ossificans progressiva;Morales-Piga;Adv Exp Med Biol.,2010

4. Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients;Connor;J Bone Joint Surg Br.,1982

5. The phenotype of fibrodysplasia ossificans progressiva;Kaplan;Clin Rev Bone Miner Metab.,2005
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