A fibrodysplasia ossificans progressiva patient with a rare missense mutation in ACVR1 detected on 18F-FDG PET/CT
Author:
Publisher
Elsevier BV
Subject
Rheumatology
Reference14 articles.
1. Fibrodysplasia ossificans progressiva: clinical and genetic aspects;Pignolo;Orphanet J Rare Dis,2011
2. Fibrodysplasia ossificans progressiva;Kaplan;Best Pract Res Clin Rheumatol,2008
3. Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1;Kaplan;Hum Mutat,2009
4. Fibrodysplasia ossificans progressiva detected on FDG PET/CT;Dua;Clin Nucl Med,2011
5. Insights from a rare genetic disorder of extra-skeletal bone formation, fibrodysplasia ossificans progressiva (FOP);Shore;Bone,2008
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