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

✍ Scribed by C. Gregson⁎; P. Hollingworth; M. Williams; K. Petrie; A. Bullock; J. Tobias; J. Triffitt

• Book ID: 116323520
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 73 KB
• Volume: 47
• Category: Article
• ISSN: 8756-3282
• DOI: 10.1016/j.bone.2010.04.615