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ACVR1 R206H receptor mutation causes fibrodysplasia ossif... | ResearchHub
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ACVR1 R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A
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Authors
Sarah Hatsell
20 more
Sarah Hatsell
•
Vincent Idone
18 more
•
Aris Economides
Published
September 2, 2015
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Journal
Science Translational Medicine
Topics
Biology
Pathology
Medicine
Internal Medicine
Nephrology
Show all topics
DOI
10.1126/scitranslmed.aac4358
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Science Translational Medicine
Topics
Biology
Pathology
Medicine
Internal Medicine
Nephrology
Show all topics
DOI
10.1126/scitranslmed.aac4358
Other Formats
PDF
