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A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date

✍ Scribed by Celia L. Gregson; Peter Hollingworth; Martin Williams; Kirsten A. Petrie; Alex N. Bullock; Matthew A. Brown; Jon H. Tobias; James T. Triffitt

Book ID: 116324084
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 651 KB
Volume: 48
Category: Article
ISSN: 8756-3282
DOI: 10.1016/j.bone.2010.10.164

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