Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg2008178.pdf
Reference36 articles.
1. Kaplan FS, Glaser DL, Hebela N, Shore EM : Heterotopic ossification. J Am Acad Orthop Surg 2004; 12: 116–125.
2. Kaplan FS, Galser DL, Shore EM et al: The phenotype of fibrodysplasia ossificans progressiva. Clin Rev Bone Miner Metab 2005; 3: 201–204.
3. Pignolo RJ, Suda RK, Kaplan FS : The fibrodysplasia ossificans progressiva lesion. Clin Rev Bone Miner Metab 2005; 3: 195–200.
4. Shore EM, Xu M, Feldman GJ et al: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat Genet 2006; 38: 525–527.
5. Shore EM, Feldman G, Xu M, Kaplan FS : The genetics of fibrodysplasia ossificans progressiva. Clin Rev Bone Miner Metab 2005; 3: 201–204.
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