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The international fibrodysplasia ossificans progressiva association.
- Source :
- Clinical Reviews in Bone & Mineral Metabolism; Sep2005, Vol. 3 Issue 3/4, p267-269, 3p
- Publication Year :
- 2005
-
Abstract
- The International Fibrodysplasia Ossificans Progressiva (FOP) Association was, founded by patient Jeannie Peeper in June of 1988 to educate patients, doctors, and the public about FOP: to raise funds and provide a patient base to support medical research into FOP: and to support patients with FOP and their families by providing a network of communication to help end the isolation that accompanies this rare and severely disabling condition. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 15348644
- Volume :
- 3
- Issue :
- 3/4
- Database :
- Complementary Index
- Journal :
- Clinical Reviews in Bone & Mineral Metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 49837565
- Full Text :
- https://doi.org/10.1385/BMM:3:3-4:267