Mutational screening ofACVR1gene in Brazilian fibrodysplasia ossificans progressiva patients
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01256.x/fullpdf
Reference14 articles.
1. Insights from a rare genetic disorder of extra-skeletal bone formation, fibrodysplasia ossificans progressiva (FOP);Shore;Bone,2008
2. Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva;Kitterman;Pediatrics,2005
3. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva;Shore;Nat Genet,2006
4. 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
5. De novo 617G-A nucleotide mutation in the ACVR1 gene in a Taiwanese patient with fibrodysplasia ossificans progressiva;Lin;J Hum Genet,2006
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