A unique case of fibrodysplasia ossificans progressiva with anACVR1 mutation, G356D, other than the common mutation (R206H)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference9 articles.
1. The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients.
2. Fibrodysplasia Ossificans Progressiva — Lessons from Rare Maladies
3. Dysregulation of the BMP-p38 MAPK Signaling Pathway in Cells From Patients With Fibrodysplasia Ossificans Progressiva (FOP)
4. Transgenic Mice Overexpressing BMP4 Develop a Fibrodysplasia Ossificans Progressiva (FOP)-Like Phenotype
5. Dysregulation of the BMP-4 Signaling Pathway in Fibrodysplasia Ossificans Progressiva
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